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Ultrasound-guided Pudendal Nerve Block for Pain After Hemorrhoidectomy

NCT05889962 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-02-26

No results posted yet for this study

Summary

The goal of this clinical trial is to investigate the effects of ultrasound-guided pudendal nerve block on postoperative pain, opioid consumption, and quality of recovery in patients receiving Ferguson hemorrhoidectomy.

Conditions

Interventions

PROCEDURE

Pudendal nerve block

Patients who are randomized in the pudendal block group will receive bilateral pudendal nerve block with ropivacaine.

PROCEDURE

Placebo block

Patients who are randomized in the placebo group will receive bilateral pudendal block with normal saline.

Sponsors & Collaborators

  • Taipei Medical University Hospital

    lead OTHER

Principal Investigators

  • Yuan-Wen Lee, MD, PhD · Taipei Medical University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-26
Primary Completion
2024-07-31
Completion
2024-09-30

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Diseases

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 NCT05889962 on ClinicalTrials.gov