Patient Guide: A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus Placebo in Pediatric Subjects, Ages 2 to 5 Years, With Functional Constipation

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 48 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05652205
Status: ACTIVE_NOT_RECRUITING
Condition: Functional Constipation (FC), Chronic Idiopathic Constipation (CIC)
Phase: PHASE3

Where You Can Participate

This study is available at 48 locations across the country.

Top locations include:
  • • Foley, Alabama
  • • Phoenix, Arizona
  • • Hot Springs, Arkansas
  • • And 45 more locations

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A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus Placebo in Pediatric Subjects, Ages 2 to 5 Years, With Functional Constipation - Join Clinical Trial NCTNCT05652205

How to Join This Clinical Trial - NCTNCT05652205

Learn how to participate in this PHASE3 trial studying an investigational therapy for Functional Constipation (FC), Chronic Idiopathic Constipation (CIC). Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Functional Constipation (FC), Chronic Idiopathic Constipation (CIC). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Functional Constipation (FC), Chronic Idiopathic Constipation (CIC)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05652205 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 48 locations. Find a study site near you:

Clinical Research Site

Foley, Alabama 36535 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85006 - United States

Status: Contact for availability

Clinical Research Site

Hot Springs, Arkansas 71913 - United States

Status: Contact for availability

Clinical Research Site

Little Rock, Arkansas 72212-4187 - United States

Status: Contact for availability

Clinical Research Site

Anaheim, California 92805 - United States

Status: Contact for availability

Clinical Research Site

Corona, California 92879-3104 - United States

Status: Contact for availability

Clinical Research Site

San Diego, California 92108 - United States

Status: Contact for availability

Clinical Research Site

Doral, Florida 33166 - United States

Status: Contact for availability

Clinical Research Site

Hollywood, Florida 33021-6030 - United States

Status: Contact for availability

Clinical Research Site

Jacksonville, Florida 32207 - United States

Status: Contact for availability

And 38 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Functional Constipation (FC), Chronic Idiopathic Constipation (CIC):

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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