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Pudendal Nerve Block in Vaginal Surgery

NCT04198714 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2024-08-12

Study results available
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Summary

The objective of this this randomized controlled study is to determine whether a pudendal nerve block at the time of vaginal surgery is associated with improved postoperative pain control and decrease opioid consumption compared to a sham pudendal nerve block in patients undergoing vaginal surgery.

Conditions

  • Nerve Block
  • Pain, Postoperative
  • Pelvic Floor Disorders
  • Pelvic Organ Prolapse
  • Pudendal Neuralgia
  • Surgery

Interventions

PROCEDURE

Pudendal block

Administration of a pudendal block at the conclusion of vaginal surgery.

Sponsors & Collaborators

  • MetroHealth Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2021-09-13
Completion
2021-09-13

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04198714 on ClinicalTrials.gov