RecruitingPhase 2NCT05953766

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

A Randomized Controlled Trial (RCT) Comparing Presacral Nerve Block Versus Sham Block on Post-operative Pain in Women Undergoing Total Laparoscopic Hysterectomy.


Sponsor

Mount Sinai Hospital, Canada

Enrollment

60 participants

Start Date

Sep 24, 2025

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Normal saline injection and a drug called Ropivacaine injection for people with post operative pain. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRopivacaine injection

Presacral nerve block using 20mL of local ropivacaine 5.0mg/ml

DRUGNormal saline injection

Sham block using 20 mL of normal saline (0.9% sodium chloride)


Locations(1)

Mount Sinai Hospital

Toronto, Ontario, Canada

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NCT05953766


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