Weill Medical College of Cornell University
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.
The purpose of this study is to develop a patient-reported outcome (PRO) instrument that can be utilized as an efficacy endpoint to assess medical and surgical treatments of chronic pelvic pain (CPP) in comparative outcomes research. This instrument will be developed consistent with Food and Drug Administration (FDA) guidance to be appropriate as an efficacy measurement in a clinical trial. The development of such a PRO measure is iterative, and this research protocol includes the qualitative research to develop a draft measure and document content validity. Content validity is first assessed…
I. First phase of study evaluation women with presumed venous origin chronic pelvic pain Inclusion Criteria : 1. Non-menopausal women ≥18 years old. a. Women who are not menstruating because of ovarian suppression therapy for CPP are eligible. 2. CPP meeting the American College of Obstetricians and Gynecologists criteria. 3. Patient pain is primarily of pelvic and/or pelvic floor origin. Patient may experience other pain symptoms, including bowel, bladder, musculoskeletal, skin allodynia and hyperalgesia, or lower extremity venous or vulvar pain. 4. Imaging demonstrating multiple tortuo…
Qualitative interviews will be performed on women with chronic pelvic pain of venous origin.
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