NCT06083597View on ClinicalTrials.gov

Development of a Patient-reported Outcome Measure for Women With Chronic Pelvic Pain

Enrolling by invitationOBSERVATIONAL
Enrollment

55

Participants

Timeline

Start Date

July 1, 2023

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2026

Conditions
Chronic Pelvic Pain SyndromePelvic Congestive Syndrome
Interventions
OTHER

Qualitative interview

Qualitative interviews will be performed on women with chronic pelvic pain of venous origin.

Trial Locations (1)

10065

Weill Cornell Medicine, New York

Sponsors

Collaborators (1)

Evidera
All Listed Sponsors
collaborator

Society of Interventional Radiology Foundation

OTHER

collaborator

Evidera

INDUSTRY

lead

Weill Medical College of Cornell University

OTHER

NCT06083597 - Development of a Patient-reported Outcome Measure for Women With Chronic Pelvic Pain | Biotech Hunter | Biotech Hunter