Status:

WITHDRAWN

Comparison of Caudal Block and Retrolaminar Block for Circumcision

Lead Sponsor:

Kanuni Sultan Suleyman Training and Research Hospital

Conditions:

Regional Anesthesia

Eligibility:

MALE

1-7 years

Phase:

NA

Brief Summary

Primary Outcome: Analgesic Efficiency: The primary outcome is the comparison of the analgesic efficacy of the retrolaminar block (RL) versus caudal block (CB) based on postoperative pain scores measu...

Detailed Description

This study is a double-blind, randomized controlled trial designed to compare the analgesic efficacy and safety of the retrolaminar block (RL) versus the caudal block (CB) in pediatric patients underg...

Eligibility Criteria

Inclusion

  • Pediatric patients aged 1 to 7 years.
  • Classified as American Society of Anesthesiologists (ASA) physical status I-II.
  • Scheduled for elective, unilateral lower abdominal surgery (e.g., orchiopexy or hydrocelectomy) combined with circumcision.
  • Patients whose parents or legal guardians provided written informed consent.

Exclusion

  • Patients younger than 1 year or older than 7 years.
  • Presence of neurological deficits.
  • Bleeding disorders.
  • History of allergy to local anesthetic drugs.
  • Presence of redness or infection at the injection site on physical examination.
  • Any congenital spinal anomalies.
  • Intellectual disabilities or psychiatric disorders.
  • Liver and/or kidney disease.
  • Patients or their guardians who declined to participate in the study.

Key Trial Info

Start Date :

September 27 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 30 2024

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT06584292

Start Date

September 27 2022

End Date

December 30 2024

Last Update

February 19 2025

Active Locations (1)

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Health Science University İstanbul Prof Dr Cemil Taşcıoğlu City Hospital

Istanbul, Okmeydanı, Turkey (Türkiye)