Investigating the analgesia effect of pudendal block with placebo after pelvic floor prolapse surgeries

Phase 2

Recruiting

• Conditions: Pelvic floor prolapse surgeries.; Incomplete uterovaginal prolapse; N81.2

• Registration Number: IRCT20231025059847N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 25

Inclusion Criteria

Women undergoing pelvic floor prolapse surgery

Exclusion Criteria

History of chronic pelvic pain
History of hypersensitivity to blocking drugs, narcotics or analgesics
Chronic use of analgesics or narcotics
Patients suffering from liver or kidney problems
Patients with simultaneous abdominal or laparoscopic surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain level after surgery. Timepoint: The day after the surgery. Method of measurement: Visual analogue scale.;Nausea. Timepoint: The day after the surgery. Method of measurement: Asking the patient how often she feels nausea.;Number of analgesics used. Timepoint: The day after the surgery. Method of measurement: Checking the number of analgesics requests in the file.