Patient Guide: BARBED vs. STANDARD Suture for Colporrhaphy at the End of Laparoscopic Hysterectomy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 1 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05833204
Status: NOT_YET_RECRUITING
Condition: Vaginal Cuff Complications
Phase: NA

Where You Can Participate

This study is available at 1 location across the country.

Top locations include:
  • • Verona,

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BARBED vs. STANDARD Suture for Colporrhaphy at the End of Laparoscopic Hysterectomy - Join Clinical Trial NCTNCT05833204

How to Join This Clinical Trial - NCTNCT05833204

Learn how to participate in this NA trial studying an investigational therapy for Vaginal Cuff Complications. Current status: NOT_YET_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Vaginal Cuff Complications
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
NOT_YET_RECRUITING
Study Identifier
NCTNCT05833204 - 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 1 locations. Find a study site near you:

Clinical Research Site

Verona, 37125 - Italy

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Vaginal Cuff Complications:

  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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