Diabetes - Escondido CA

  • STATUS
    Recruiting
Updated on 16 September 2022

Summary

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 encourage YOU to leave us your contact information at our volunteer page: myAMCR.com or call us at 877-567-AMCR (2627) with any questions.
We truly appreciate your consideration,  Your AMazing CRew

Description

Eligible participants may receive study related medications, diabetes supplies, medical care at no cost and compensation for time.

Details
Condition Diabetes Mellitus Types I and II, Diabetes (Adults, Pediatric and Seniors)
Clinical Study IdentifierTX211447
Last Modified on16 September 2022

Eligibility

Yes No Not Sure

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
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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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