With your help, we can help advance medical knowledge and improve the health and well-being of countless others.
Our goal is to assist the pharmaceutical and medical device industries develop new and effective products to treat a multitude of medical conditions and illnesses. We perform this important work through the administration of clinical trials.
Please consider joining us in this effort. Our experienced and professional clinical research staff are highly qualified and fully committed to engaging you and your primary care physician as informed partners in everything we do.
Available Studies
See if you pre-qualify for any of the research studies we are now conducting in your area by following one of the links below.
AMR Newton is conducting a Clinical Trial of an Investigational Once-Daily ORAL Medication for Type 2 Diabetics with Cardiovascular Risk.
Qualified participants:
· Are 18 and Older
· Have either Heart Disease (incl. heart attack, stent, bypass surgery, heart failure, among others), Peripheral Artery Disease, Kidney Disease, or have had a Stroke or TIA
AND
· Have an A1C of 7 to 10.5 (Stable Treatment of One to Three Oral Medications for Diabetes) Note: If Taking Metformin, ≥1500 mg/day is required.
· Meet Other Study Requirements (Use of Insulin and/or Some Newer Injectable Diabetic Medications is Prohibited)
Reimbursement is available for time and travel. Contact AMR Newton at 316-283-0828.
If you have Type 1 or Type 2 Diabetes, you may qualify for a clinical research study happening at AMR Wichita West.
Qualified participants must:
· be ages 18 and older
· have Type 1 or Type 2 diabetes
· be diagnosed with Diabetic Gastroparesis
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related medical examinations and lab work
· the investigational medication or placebo
Compensation is available up to $725.00 for time and travel. Insurance is not required. Contact AMR Wichita West at 316-867-6329 to learn more.
AMR Wichita East is currently enrolling in a pediatric migraine clinical research study.
Qualified participants will:
· Be 6 to 17 years of age
· Meet other study criteria
Qualified participants will receive at no cost:
· All study-related medical exams
· Study-related Lab tests
· Investigational medication or placebo
If you are interested in learning about this study, please contact our office. Compensation for time and travel may be provided up to $225.00. For a research trial consultant, call 316-867-6329.
AMR is currently accepting volunteers to participate in a gout clinical research study. Qualified participants are those ages 19 to 69 who meet other study criteria. Qualified participants will receive all study-related care and the investigational medication or placebo at no cost. Compensation may be available for study-related time and travel. To learn more, call AMR at 316-283-0828 today!
According to the CDC, Atrial Fibrillation, often called AFib or AF, is the most common type of treated heart arrhythmia. An arrhythmia is when the heart beats too slowly, too fast, or in an irregular way. AFib increases your risk of having a stroke due to the formation of blood clots. Oral anticoagulants (sometimes called “blood thinners”) can be used to prevent stroke associated with AFib. AMR Wichita East is currently conducting a clinical research study of an investigational treatment to prevent stroke in patients who are diagnosed with AFib but are unsuitable for oral anticoagulation.
Qualified participants must:
· be age 65 or older
· be diagnosed with Afib
· be unsuitable for oral anticoagulation, by your responsible physician(s) or by your own decision
· have conditions associated with a risk of bleeding
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related medical examinations and lab work
· the investigational treatment or placebo
Compensation is available up to $2,875.00 for time and travel. Insurance is not required. Contact AMR Wichita East at 316-867-6329 to participate in this clinical research study.
AMR is currently accepting volunteers to participate in a Psoriatic Arthritis clinical research study. Qualified participants are those ages 18 and older who meet other study criteria. Qualified participants will receive all study-related care and the investigational treatment or placebo at no cost. Compensation may be available for study-related time and travel.
When a child gets RSV or Respiratory Syncytial Virus, it can cause more severe infections such as bronchiolitis and pneumonia. In fact, it is the most common cause of bronchiolitis and pneumonia in children younger than one year of age. With no approved vaccine available, AMR Newton continues to study investigational vaccines to prevent and protect from RSV and we are currently enrolling in an investigational Intranasal Pediatric RSV Vaccine Research Study.
Qualified participants must:
· be ages 6 to 59 months of age
· meet other study criteria
Qualified participants will receive all study-related care and the investigational Intranasal vaccine or placebo at no cost. Compensation is available up to $1,000.00. Insurance is not required. Protecting our children protects everyone. Call AMR Newton at 316-283-0828 to learn more.
If you suffer from Elevated Triglyceride Levels, you may qualify for an investigational clinical research study at AMR Newton.
Qualified participants must:
· be ages 18 to 79
· be on statin or non-statin lipid-altering therapy
· meet other study criteria
Receive all study-related care and investigational medication or placebo at no cost. Compensation for time and travel is available up to $1,225.00. Insurance is not required. To learn more, call AMR Newton at 316-283-0828 today.
AMR is currently accepting volunteers to participate in a Type 2 Diabetic clinical research study. Qualified participants are those ages 18 and older who meet other study criteria. Qualified participants will receive all study-related care and the investigational medication or placebo at no cost. Compensation may be available for study-related time and travel. To learn more, call AMR at 316-283-0828 today!
Cardiovascular disease is risky business! That’s why AMR Wichita East is conducting a clinical trial of an investigational medication to potentially reduce major adverse cardiovascular events in those with a previous history of adverse cardiovascular events and in those who are at high cardiovascular risk.
Qualified participants must:
· be ages 18 and older with a history of a major cardiovascular event Or
· be ages 50 and older who are at high risk for having their first major cardiovascular event
· meet other study criteria
Qualified participants will receive:
· all study-related care and the investigational medication or placebo at no cost
· compensation up to $2,550.00 for time and travel
Learn more by calling AMR Wichita East at 316-867-6329 today!
Severe hypertriglyceridemia is a common condition characterized by triglyceride levels more than three times the normal level. This can lead to serious conditions such as cardiovascular disease and acute pancreatitis. If you have been diagnosed with severe hypertriglyceridemia or SHTG, you may qualify for an investigational clinical research study at AMR Wichita West.
Qualified participants are ages 22 and older and meet other study criteria. Qualified participants will receive all study-related care and investigational medication or placebo at no cost. Compensation is available up to $1,850.00 and insurance is not required.
Call AMR Wichita West at 316-867-6329 to learn more today.
Diabetic Peripheral Neuropathic Pain: the most common type of diabetic neuropathy that affects the feet and legs first. It significantly impacts the quality of life in walking ability, sleep, work, and general activity. Currently, there are only four medications approved by the FDA for DPNP and clinical guidelines recommend pain relief through antidepressants, opioids, and topical medications.
AMR Wichita West is evaluating an investigational medication in adult participants with Diabetic Peripheral Neuropathic Pain to potentially lessen pain intensity.
Qualified participants must:
· be 18 and older
· have Type 1 Diabetes or Type 2 Diabetes diagnosed at least six months prior
· be on a stable diabetes treatment
· be willing to have a metformin dose modification
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related care and health monitoring
· the investigational medication or placebo
Compensation is available up to $1,533.00 for time and travel. To learn more, call AMR Wichita West at 316-867-6329 today.
AMR El Dorado is conducting a study to test an investigational drug on cardiovascular safety for people who are overweight or obese.
Qualified participants must:
· be ages 18 and older
· have a BMI of 27 or greater
· have cardiovascular disease, chronic kidney disease, or at least two risk factors for cardiovascular disease such as hypertension, dyslipidemia, Type 2 Diabetes, or Non-alcoholic steatohepatitis (NASH)
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related care
· the investigational drug or placebo
Compensation for time and travel may be provided. Learn more by calling AMR El Dorado at 316-600-5127 today!
AMR Wichita East is conducting a study to test an investigational drug on cardiovascular safety for people who are overweight or obese.
Qualified participants must:
· be ages 18 and older
· have a BMI of 27 or greater
· have cardiovascular disease, chronic kidney disease, or at least two risk factors for cardiovascular disease such as hypertension, dyslipidemia, Type 2 Diabetes, or Non-alcoholic steatohepatitis (NASH)
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related care
· the investigational drug or placebo
Compensation for time and travel may be provided. Learn more by calling AMR Wichita East at 316-867-6329 today!
AMR Newton is conducting a study to test an investigational drug on cardiovascular safety for people who are overweight or obese.
Qualified participants must:
· be ages 18 and older
· have a BMI of 27 or greater
· have cardiovascular disease, chronic kidney disease, or at least two risk factors for cardiovascular disease such as hypertension, dyslipidemia, Type 2 Diabetes, or Non-alcoholic steatohepatitis (NASH)
· meet other study criteria
Qualified participants will receive at no cost:
· all study-related care
· the investigational drug or placebo
Compensation for time and travel may be provided. Learn more by calling AMR Newton at 316-283-0828 today!
Painful Lumbosacral Radiculopathy (PLSR) clinical study is happening now at AMR. Lumbosacral radiculopathy, commonly known as sciatica, is a term used to describe a pain syndrome caused by compression or irritation of nerve roots in the lower back leading to pain in the leg. It can be caused by lumbar disc herniation, degeneration of the spinal vertebra, and narrowing of the foramen from which the nerves exit the spinal canal.
Qualified participants must:
· be 18 to 70
· have been diagnosed with Lumbosacral Radiculopathy at least three months prior to study start
· meet other study criteria
Qualified participants will:
· receive all study-related care and investigational medication or placebo at no cost;
· receive compensation up to $1,600.00 for study-related time and reimbursement for travel.
To learn more, call AMR at 316-867-6329.
No matter how young you are, migraines can be painful and debilitating. Learn more about a pediatric migraine treatment clinical study of an investigational treatment at AMR Wichita West.
To be eligible, participants must:
· be ages 6 to 17
· have a history of migraine for at least six months
· meet other study criteria
All study-related visits and investigational medication will be provided at no cost. Compensation is available up to $300.00 for this three-visit study. Insurance is not required. Call AMR Wichita West at 316-867-6329.
AMR El Dorado is currently seeking healthy volunteers to participate in a clinical research study of an investigational medication to prevent Botulism.
Qualified participants must:
• be a healthy adult 18 to 65 years of age
• meet other study criteria
Qualified participants will receive at no cost:
• all study-related medical exams
• lab tests
• injection of the investigational medication or placebo
Reimbursement for time and study-related travel is available up to $2,450.00. Insurance is not required.
To see if you qualify, call:
AMR El Dorado at 316-600-5127
AMR Newton is currently seeking healthy volunteers to participate in a clinical research study of an investigational medication to prevent Botulism.
Qualified participants must:
• be a healthy adult 18 to 65 years of age
• meet other study criteria
Qualified participants will receive at no cost:
• all study-related medical exams
• lab tests
• injection of the investigational medication or placebo
Reimbursement for time and study-related travel is available up to $2,450.00. Insurance is not required.
To see if you qualify, call:
AMR Newton at 316-283-0828
AMR Wichita East is currently seeking healthy volunteers to participate in a clinical research study of an investigational medication to prevent Botulism.
Qualified participants must:
• be a healthy adult 18 to 65 years of age
• meet other study criteria
Qualified participants will receive at no cost:
• all study-related medical exams
• lab tests
• injection of the investigational medication or placebo
Reimbursement for time and study-related travel is available up to $2,450.00. Insurance is not required.
To see if you qualify, call:
AMR Wichita East at 316-867-6329
AMR Wichita West is currently seeking healthy volunteers to participate in a clinical research study of an investigational medication to prevent Botulism.
Qualified participants must:
• be a healthy adult 18 to 65 years of age
• meet other study criteria
Qualified participants will receive at no cost:
• all study-related medical exams
• lab tests
• injection of the investigational medication or placebo
Reimbursement for time and study-related travel is available up to $2,450.00. Insurance is not required.
To see if you qualify, call:
AMR Wichita West at 316-867-6329
AMR is currently accepting volunteers to participate in an RSV vaccine clinical research study. Qualified participants are those ages 60 and older who meet other study criteria. Qualified participants will receive all study-related care and the investigational medication or placebo at no cost. Compensation may be available up to $400.00 for study-related time and travel.
To learn more, call AMR at 316-867-6329 today!
AMR Wichita East is seeking healthy adults ages 18 and older for an investigational bird flu vaccine clinical study. Qualified participants will receive all study-related care and the investigational vaccine at no cost. Reimbursement for study-related time and travel is available up to $1,050.00.
Qualified participants must:
• be adults ages 18 and older
• be considered healthy
• meet other study eligibility criteria
To learn more, call AMR Wichita East today at 316-867-6329.
AMR Newton would like to invite you to participate in an Influenza Vaccine clinical research study happening now.
Qualified participants must:
• be 50 to 64 years of age
• meet additional study criteria
Receive all study-related care and the study vaccine at no cost. Compensation may be available for time and travel.
To learn more, call AMR at 316-283-0828.
Frequently Asked Questions
In Phase I trials, researchers test an experimental drug or treatment in a small group of people (20-80) for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
In Phase II trials, the experimental study drug or treatment is given to a larger group of people (100-300) to see if it is effective and to further evaluate its safety.
In Phase III trials, the experimental study drug or treatment is given to large groups of people (1,000-3,000) to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the experimental drug or treatment to be used safely.
A protocol is a study plan on which all clinical trials are based. The plan is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study. While in a clinical trial, participants following a protocol are seen regularly by the research staff to monitor their health and to determine the safety and effectiveness of their treatment.
Clinical trials that are well-designed and well-executed are the best approach for eligible participants to:
Play an active role in their own health care.
Gain access to new research treatments before they are widely available.
Obtain expert medical care at leading healthcare facilities during the trial.
Help others by contributing to medical research.
Risks
There are risks to clinical trials.
There may be unpleasant, serious or even life-threatening side effects to experimental treatment.
The experimental treatment may not be effective for the participant.
The protocol may require more of their time and attention than would a non-protocol treatment, including trips to the study site, more treatments, hospital stays or complex dosage requirements.
Some clinical trials involve more tests and doctor visits than the participant would normally have for an illness or condition. For all types of trials, the participant works with a research team. Clinical trial participation is most successful when the protocol is carefully followed and there is frequent contact with the research staff.
All clinical trials have guidelines about who can participate. Using inclusion/exclusion criteria is an important principle of medical research that helps to produce reliable results. The factors that allow someone to participate in a clinical trial are called “inclusion criteria” and those that disallow someone from participating are called “exclusion criteria”. These criteria are based on such factors as age, gender, the type and stage of a disease, previous treatment history, and other medical conditions. Before joining a clinical trial, a participant must qualify for the study. Some research studies seek participants with illnesses or conditions to be studied in the clinical trial, while others need healthy participants. It is important to note that inclusion and exclusion criteria are not used to reject people personally. Instead, the criteria are used to identify appropriate participants and keep them safe. The criteria help ensure that researchers will be able to answer the questions they plan to study
Participants in clinical trials can play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.
Although there are many definitions of clinical trials, they are generally considered to be biomedical or health-related research studies in human beings that follow a predefined protocol. ClinicalTrials.gov includes both interventional and observational types of studies. Interventional studies are those in which the research subjects are assigned by the investigator to a treatment or other intervention, and their outcomes are measured. Observational studies are those in which individuals are observed and their outcomes are measured by the investigators.
Volunteer Form
By volunteering for clinical studies, you authorize AMR to store your personal information on file. In accordance with HIPAA regulations, AMR will never share your information with anyone.
Respiratory Syncytial Virus
It is estimated that more than 177,000 older adults are hospitalized and 14,000 of them die in the US due to RSV infections per year. In 2018, more elder Americans died from RSV infection than the common flu.
To learn more, call our enrollment line:
Refer-A-Friend
Earn extra cash* by recommending a friend to us and receive up to $100 for each friend you refer!
* Some restrictions apply. Not all studies are eligible for the Refer-A-Friend program. Ask an AMR representative for details.
Refer-A-Friend
Step 1
Fill out the Refer-A-Friend form. You can download the form here or pick one up at one of our offices. The referrer (you) must fill out the form.
Step 2
Your friend or family member brings the completed referral form to CRC on their first visit to our office and gives it to a staff member upon checking in.
Step 3
If your referral qualifies for and completes all visits for the study, you (the referrer) will earn $100 upon study completion.
Refer-A-Friend
Step 1
Fill out the Refer-A-Friend form. You can download the form here or pick one up at one of our offices. The referrer (you) must fill out the form.
Step 2
Your friend or family member brings the completed referral form to CRC on their first visit to our office and gives it to a staff member upon checking in.
Step 3
If your referral qualifies for and completes all visits for the study, you (the referrer) will earn $100 upon study completion.
Refer-A-Friend
Step 1
Fill out the Refer-A-Friend form. You can download the form here or pick one up at one of our offices. The referrer (you) must fill out the form.
Step 2
Your friend or family member brings the completed referral form to CRC on their first visit to our office and gives it to a staff member upon checking in.
Step 3
If your referral qualifies for and completes all visits for the study, you (the referrer) will earn $100 upon study completion.
Refer-A-Friend
Step 1
Fill out the Refer-A-Friend form. You can download the form here or pick one up at one of our offices. The referrer (you) must fill out the form.
Step 2
Your friend or family member brings the completed referral form to CRC on their first visit to our office and gives it to a staff member upon checking in.
Step 3
If your referral qualifies for and completes all visits for the study, you (the referrer) will earn $100 upon study completion.
