Has Diabetes Affected Your Life?

Updated on 29 November 2022


Be part of a new approach to Diabetes care! AMCR Institute is currently recruiting for clinical trials to evaluate medical devices and investigational medications for pediatric and adult individuals with Type 1, Type 2 Diabetes, and obesity. AMCR Institute's team is committed to providing superior service to our volunteers and partners. Clinical research studies are vital to improving the quality of care for those with chronic conditions. Patients who volunteer at AMCR Institute contribute to the discovery of new therapies to treat and possibly cure their illness. You are THE important link to cutting-edge research that can benefit people long before a device or medication becomes available in the healthcare marketplace.
We truly appreciate your consideration, Your Amazing Crew


Do YOU Want To Help Change How Diabetes Affects Future Generations? Participate In A Clinical Research Trial.
AMCR Institute is looking for volunteers to participate in ongoing clinical trials.

Condition Diabetes Mellitus Types I and II, Diabetes Mellitus, Type 1, Type 2, Indikation: Diabetes - Typ II, Diabetes Mellitus Type 2, Diabetes Prevention, Diabetes and Hypertension, Obesity
Clinical Study IdentifierTX307749
Last Modified on29 November 2022


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Inclusion Criteria

Diagnosed with pre-diabetes, Type 1 or Type 2 Diabetes, and/or obesity
Each study has specific requirements such as age, sex, and a current diagnosis of the medical condition, medical treatment, lab results, etc
Live within 50 Miles of Escondido, CA
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

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