Houston, TXNCT06827977Now EnrollingIRB Ready

Constipation Clinical Trial in Houston, TX

Access cutting-edge constipation treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by The University of Texas Health Science Center, Houston

Quick Self-Assessment

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Expert Care in Houston

Access constipation specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related constipation treatment provided free

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Check if you qualify for this constipation clinical trial in Houston, TX

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Houston site if eligible
  4. 4Begin participation

About This Constipation Study in Houston

The purpose of this study is to characterize the intestinal flora in subjects with systemic sclerosis-related constipation and/or significant bloating and to determine safety and trends in improvements in the diversity of colonic microbiome and patient symptoms following the administration of either frozen or lyophilized PRIM-DJ2727 microbiota.

Sponsor: The University of Texas Health Science Center, Houston

Who Can Participate

Inclusion Criteria

Are seen in the UT Houston Scleroderma Center (UTHSC)
Meet 2013 American college of rheumatology (ACR)/European league against rheumatism (EULAR) criteria or CREST criteria for SSc
Meet Rome IV criteria for constipation and/or significant bloating
Subject willing to sign an informed consent form
Subject deemed likely to survive for ≥ 1 year after enrollment
Able to follow study procedure and follow-up
Sexually active male and female subjects of childbearing potential must agree to use an effective method of birth control during the treatment and follow-up period
Female subjects of childbearing potential must have a negative pregnancy test in the 72 hours before the procedure
Subjects who agree to adhere to a stable diet for at least 4 weeks before joining the study and throughout the study
Subjects must have an attending physician who will provide non-transplant care for the subject

Exclusion Criteria

Subjects with constipation and/or significant bloating from causes not attributed to SSc as determined by the treating physician (e.g., inflammatory bowel disease, medication, significant diabetes, or hypothyroidism, etc.)
Subjects unwilling to stop taking probiotic supplements during the duration of the study
Subjects that have post-total or hemicolectomy or the presence of a colostomy
Subjects unable to tolerate microbiome transplant via enema for any reason or swallow capsules
Subjects requiring systemic antibiotic therapy 4 weeks before the study
If subjects are on immunosuppression, the immunosuppression dose should be stable for at least 4 weeks before study enrollment

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Houston?

Yes, this clinical trial (NCT06827977) has an active research site in Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Constipation Treatment Options in Houston, TX

If you're searching for constipation treatment options in Houston, TX, this clinical trial (NCT06827977) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced constipation specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all constipation clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Houston, TX