Foley, ALNCT07382167Now EnrollingIRB Ready

Chronic Idiopathic Constipation (CIC) Clinical Trial in Foley, AL

Access cutting-edge chronic idiopathic constipation (cic) treatment through this clinical trial at a research site in Foley. Study-provided care at no cost to qualified participants.

Sponsored by Ardelyx

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in Foley

Access chronic idiopathic constipation (cic) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic idiopathic constipation (cic) treatment provided free

Apply for This Foley Location

Check if you qualify for this chronic idiopathic constipation (cic) clinical trial in Foley, AL

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Why Participate?

  • No-Cost Study Care

  • Local to Foley

    Convenient for AL 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 Foley site if eligible
  4. 4Begin participation

About This Chronic Idiopathic Constipation (CIC) Study in Foley

This is a 26-week, multi-center, randomized, double-blind, placebo-controlled study with a 4-week treatment-free Safety Follow-up period to assess the safety and efficacy of tenapanor (5 mg, 25mg, and 50 mg) in adult patients with Chronic Idiopathic Constipation (CIC) when administered twice daily for 26 consecutive weeks.

Sponsor: Ardelyx

Who Can Participate

Inclusion Criteria

Patients ≥18 to ≤80 years old at the Screening visit (Visit 1).
Meet the Rome IV Diagnostic Criteria for functional constipation.
Females of non-childbearing potential, or agree to the use of an acceptable means of contraception for up to 30 days following the last dose of study medication.
Males must agree to use an appropriate method of barrier contraception or have documented surgical sterilization.
Meets the entry criteria assessed during the Screening period.
Ability to understand and provide input on the assessments in the eDiary.
Provide written informed consent before the initiation of any study-specific procedures.
Must agree to have daily access to eDiary via a computer, tablet or smart phone

Exclusion Criteria

Loose or watery stool in the absence of any medication that is known to affect stool consistency for \>25% of bowel movements (BMs) during the 3 months prior to the Screening visit
Fecal impaction within 6 months prior to the Screening visit
Unexplained and clinically significant alarm symptoms.
Functional diarrhea as defined by Rome IV criteria
IBS with constipation (IBS-C), IBS with diarrhea (IBS-D), mixed IBS (IBS-M), or unsubtyped IBS as defined by Rome IV criteria
Diagnosis or treatment of any clinically symptomatic abnormality of the GI tract or active disease within 6 months prior to the Screening visit
Patient with central nervous system disorder
Use of prohibited medications defined by protocol
Patient has a history or current evidence of laxative abuse
Hepatic dysfunction
Positive HIV, hepatitis B or hepatitis C test at screening
Positive urinary drug test at Screening, with the exception of cannabis and cannabidiol (CBD)
Any evidence of or treatment of malignancy within 1 year prior to the Screening visit
Any surgery on the stomach, small intestine or colon; appendectomy or cholecystectomy are not excluded unless within 60 days prior to the Screening visit
Pregnant women or women planning to become pregnant during trial participation
A major psychiatric disorder that has required hospitalization in the last year prior to the Screening visit.
Alcohol or substance abuse within 1 year prior to the Screening visit
Participation in other clinical trials within 1 month prior to the Screening visit
Clinical evidence of significant disease that may interfere with the patient's successful completion of the trial

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 Foley?

Yes, this clinical trial (NCT07382167) has an active research site in Foley, AL 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.

Chronic Idiopathic Constipation (CIC) Treatment Options in Foley, AL

If you're searching for chronic idiopathic constipation (cic) treatment options in Foley, AL, this clinical trial (NCT07382167) 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 Foley research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic idiopathic constipation (cic) 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 chronic idiopathic constipation (cic) clinical trials near you to find additional studies recruiting in your area.

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