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

NCT06083597 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 55

Last updated 2025-12-18

No results posted yet for this study

Summary

The purpose of this study is to develop a patient questionnaire that can be utilized to assess the benefit of treatments of chronic pelvic pain in research studies.

The information collected from a series of patient interviews will lead to the development of a questionnaire that accounts for the full impact of chronic pelvic pain from an affected woman's perspective.

Conditions

  • Chronic Pelvic Pain Syndrome
  • Pelvic Congestive Syndrome

Interventions

OTHER

Qualitative interview

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

Sponsors & Collaborators

  • Society of Interventional Radiology Foundation

    collaborator OTHER

  • Evidera

    collaborator INDUSTRY

  • Weill Medical College of Cornell University

    lead OTHER

Principal Investigators

  • Neil M Khilnani, MD · Weill Medical College of Cornell University

  • Robin Pokrzywinski, PhD · Evidera

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-07-01
Primary Completion
2026-12-31
Completion
2026-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06083597 on ClinicalTrials.gov