Patient Guide: A Study of Orforglipron in Female Participants With Stress Urinary Incontinence Who Have Obesity or Overweight

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 115 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07202884
Status: NOT_YET_RECRUITING
Condition: Urinary Incontinence,Stress
Phase: PHASE3

Where You Can Participate

This study is available at 115 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Mobile, Alabama
  • • Mesa, Arizona
  • • And 112 more locations

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A Study of Orforglipron in Female Participants With Stress Urinary Incontinence Who Have Obesity or Overweight - Join Clinical Trial NCTNCT07202884

How to Join This Clinical Trial - NCTNCT07202884

Learn how to participate in this PHASE3 trial studying an investigational therapy for Urinary Incontinence,Stress. Current status: NOT_YET_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Urinary Incontinence,Stress. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Urinary Incontinence,Stress
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
NOT_YET_RECRUITING
Study Identifier
NCTNCT07202884 - 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 115 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35233 - United States

Status: Contact for availability

Clinical Research Site

Mobile, Alabama 36608 - United States

Status: Contact for availability

Clinical Research Site

Mesa, Arizona 85206 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90057 - United States

Status: Contact for availability

Clinical Research Site

Montebello, California 90640 - United States

Status: Contact for availability

Clinical Research Site

Tustin, California 92780 - United States

Status: Contact for availability

Clinical Research Site

Lakewood, Colorado 80228 - United States

Status: Contact for availability

Clinical Research Site

Fort Myers, Florida 33912 - United States

Status: Contact for availability

Clinical Research Site

Lake Worth, Florida 33461 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33186 - United States

Status: Contact for availability

And 105 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 Urinary Incontinence,Stress:

  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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