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Pudendal Nerve Block for Hemorrhoidectomy

NCT04251884 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 49

Last updated 2022-03-11

Study results available
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Summary

Patients undergoing Milligan-Morgan hemorrhoidectomy will be randomized to receive or not the pudendal nerve block after the spinal anesthesia.

Conditions

Interventions

PROCEDURE

Local anesthetic (ropivacaine)

Patients randomized in the treatment arm will receive a sonography-guided pudendal nerve block

Sponsors & Collaborators

  • Francesco Mongelli

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2019-12-29
Completion
2020-01-30

Countries

  • Switzerland

Study Locations

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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 NCT04251884 on ClinicalTrials.gov