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Pudendal Block Versus Caudal Block for Hypospadias

NCT02390388 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2015-08-26

No results posted yet for this study

Summary

The aim of this prospective randomized study is to assess the analgesic efficacy and duration of Pudendal block compared with Caudal block for pediatric patients undergoing hypospadias surgery concerning intraoperative analgesic and also postoperative total analgesic consumption within 24 hours.

Conditions

Interventions

PROCEDURE

pudendal nerve block

nerve stimulator-guided Pudendal block

PROCEDURE

caudal block

caudal block

Sponsors & Collaborators

  • Ayse Cigdem Tutuncu

    collaborator OTHER

  • Senol Emre

    collaborator UNKNOWN

  • Fatis Altindas

    collaborator UNKNOWN

  • Kaya, Guner, M.D.

    collaborator INDIV

  • Istanbul University

    lead OTHER

Principal Investigators

  • Guner Kaya, Prof. · Istanbul University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Max Age
10 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2015-05-31
Completion
2015-05-31

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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 NCT02390388 on ClinicalTrials.gov