Clinical Trial

Presacral Nerve Block Versus Sham Block on Post-operative Pain for Total Laparoscopic Hysterectomy

Recruiting Phase 2
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Record status
This record was last updated April 6, 2026 (before its estimated July 2026 completion). Its status may not reflect the trial's current state.
Summary
The study is a single-center parallel group randomized controlled trial comparing the administration of a presacral nerve block using 20mL of local ropivacaine 5.0mg/ml versus 20mL of normal saline (sham block) on post-operative pain following total laparoscopic hysterectomy.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2023-07-12; most recent amendment 2026-03-31.
Status change: Not Yet Recruiting → Recruiting 2025-07-28
Trial Details
NCT Number NCT05953766
Lead Sponsor Mount Sinai Hospital, Canada
Conditions Post-operative Pain
Enrollment 60 participants
Start Date 2025-09-24
Primary Completion 2026-07 (estimated)
Study Completion 2026-07 (estimated)
Updated on ClinicalTrials.gov 2026-04-06