Clinical Trial

Effect of Pain Vigilance on Pain, Bladder-Bowel Function and Sexual Life

Completed
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Summary
The aim of this study to investigate the effect of preoperative pain hypervigilance on postoperative pain, bladder-bowel symptoms and sexual life after vaginal surgery and to compare these parameters before and after surgery. Pain vigilance (Pain Vigilance and Awareness Questionnaire-PVAQ), pain catastrophizing (Pain Catastrophizing Scale-PCS), bladder-bowel function (Australian Pelvic Floor Questionnaire-APFQ), and sexual function (Female Sexual Function Index (FSFI)) of women were recorded before and after surgery. Visual analogue scales were used to assess the postoperative pain intensity.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2025-07-14; most recent amendment 2026-02-26.
Status change: Not Yet Recruiting → Completed 2026-02-26
Trial Details
NCT Number NCT07065188
Lead Sponsor Ordu University
Conditions Vaginal Surgery
Enrollment 77 participants
Start Date 2025-10-01
Primary Completion 2026-02-05 (estimated)
Study Completion 2026-02-26 (estimated)
Updated on ClinicalTrials.gov 2026-02-27