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

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

Inclusion Criteria2

  • years of age or older
  • Undergoing total laparoscopic hysterectomy

Exclusion Criteria8

  • Previous presacral neurectomy
  • Concurrent surgical procedure other than salpingectomy and/or oophorectomy
  • Gynecological cancer beyond stage 1 disease
  • BMI > 50
  • Chronic opioid consumption
  • Fibromyalgia
  • Language barrier
  • Inability to communicate and provide consent

Interested in this trial?

Get notified about updates and connect with the research team.

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

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05953766