Research study for volunteers at least 18 years of age who are currently experiencing symptoms of chronic constipation

  • STATUS
    Recruiting
Updated on 25 March 2021

Summary

Research study for volunteers at least 18 years of age who are currently experiencing symptoms of chronic constipation

Description

This is a research study for chronic idiopathic constipation. Subjects who meet the inclusion criteria will be entered into up to a 9 day treatment period. Patients will either receive the product under study or the marketed equivalent or placebo. Medication will be administered orally twice daily.

Patient Inclusion Criteria:

  • Male and non-pregnant females 18 years of age and older
  • Chronic idiopathic constipation defined as, on average <3 bowel movements per week for the past 6 months
  • Confirmation of chronic constipation by a daily diary during the 14 day lead-in period

  • Pregnancy or breast feeding
  • Documented bowel obstruction
  • Crohn’s disease, ulcerative colitis
  • History of bowel resection
  • Regular use of medications known to cause constipation
  • Unstable hypothyroidism, Parkinson’s disease, multiple sclerosis or spinal cord disorder
  • Any hospitalization for any gastrointestinal or abdominal surgical procedure 3 months prior to dosing

Patient Exclusion Criteria:

    Details
    Clinical Study IdentifierTX135472
    Last Modified on25 March 2021

    Eligibility

    How to participate?

    Step 1 Connect with a site
    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.

    You are contacting

    Investigator Avatar
    Name

    Primary Contact

    site
    Name

    0/250
    Preferred Language
    Other Language
    Please verify that you are not a bot.

    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

    Similar trials to consider

    Loading...

    Not finding what you're looking for?

    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.

    Sign up as volunteer

    user name

    Added by • 

     • 

    Private

    Reply by • Private
    Loading...

    Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

      The passcode will expire in None.
    Loading...

    No annotations made yet

    Add a private note
    • abc Select a piece of text from the left.
    • Add notes visible only to you.
    • Send it to people through a passcode protected link.
    Add a private note