If you are at least 18 years of age, have been diagnosed and currently treating for type 2 diabetes, please contact Coastal Carolina Research Center about our new medical research study.

  • STATUS
    Recruiting
Updated on 25 March 2021

Summary

If you are at least 18 years of age, have been diagnosed and currently treating for type 2 diabetes, please contact Coastal Carolina Research Center about our new medical research study.

Description

The purpose of this research study is to determine the safety and effectiveness of an investigational medication on blood sugar levels. The study will assess any change in blood sugar and weight loss. If you are eligible and decide to volunteer you can expect 14 office visits over a period of up to 122 weeks

All research study-related care is provided to qualified participants at no cost including:

  • Investigational medication
  • Physical exam
  • Lab work including A1C measurement
  • ECG
  • Diet and exercise counseling and monitoring

Monetary compensation is available for those who volunteer and qualify. No health insurance is required.

If you are interested in learning more about this study, please contact Coastal Carolina Research Center at 856-3784 (856-DRUG). You may also text STUDY to 72727 or apply online at www.coastalcarolinaresearch.com. Referrals to your family members, friends or co-workers would be appreciated as we cannot do our work without the support of the Lowcountry community.

Details
Condition Diabetes Mellitus, Type 2
Clinical Study IdentifierTX138818
Last Modified on25 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

To qualify participants must
Be male or female at least 18 years of age
Be currently taking medication for diabetes not including insulin
Females who are currently using or willing to use reliable contraceptives during the course of the study
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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.

Learn more

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.

Learn more

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

Learn more

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