Are you interested in a clinical research study for your type 2 diabetes?

  • STATUS
    Recruiting
Updated on 8 November 2020

Summary

Are you interested in a clinical research study for your type 2 diabetes?

Description

To see if you may be eligible to participate in an OMNEON Clinical Research Program, you will be asked to answer some questions about your health history and current conditions. The information you provide will be kept confidential and will not be shared without your permission or except as required by law. We will provide it only to personnel at study sites that may contact you about the possibility of your participation in this clinical research study if we determine that you might be eligible.

If you are eligible and willing to participate, you will first be asked to visit a medical site near you. The purpose of the visits is to determine if you meet all of the entry criteria for the study. Qualifying to participate in any one of the OMNEON Clinical Research Program will depend on a range of criteria. Before deciding whether to participate, you should make sure you understand the risks with the study. These will be explained to you by the study doctor.

The study staff will perform study-related physical examinations and collect blood and urine samples for laboratory testing. You will receive study medication and study-related medical care at no charge. Participants will also receive a glucose meter and related supplies to measure blood sugar levels at home.

For more information please contact MD CLINICAL 954-455-5757 ext 111

Details
Clinical Study IdentifierTX137131
Last Modified on8 November 2020

Eligibility

How to participate?

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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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