Irritable Bowel Syndrome with Constipation Clinical Trial

  • STATUS
    Recruiting
Updated on 8 November 2020

Summary

Irritable Bowel Syndrome with Constipation Clinical Trial

Description

Are you currently experiencing abdominal pain and constipation due to your Irritable Bowel Syndrome Condition?

We are conducting a clinical research study on an investigational study medication for people with Irritable Bowel Syndrome with constipation (IBS-C)

You may qualify if you are:

  • 18-85 years of age
  • Currently experiencing abdominal pain and constipation due to your Irritable Bowel Syndrome condition
  • Able and willing to make daily reports on your symptoms throughout the study
  • Able and willing to participate in the clinical research study for approximately 18 weeks

*additional criteria may apply

Eligible participants will receive at no cost:

  • Investigational Medication
  • Study related care
  • Compensation for travel and possible other reimbursement

For more information, please contact (619) 589-4103.

Details
Condition Constipation
Clinical Study IdentifierTX145293
Last Modified on8 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Are between 18 to 75 years old
Have been diagnosed with irritable bowel syndrome with constipation
Experienced abdominal pain or discomfort for at least 3 days per month in the last 3 months

Exclusion Criteria

Excluded who is pregnant, nursing, or planning to become pregnant during study participation
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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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