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High Volume Caudal Study

High Volume Caudal Study

Recruiting
3 years and younger
Male
Phase N/A

Overview

The primary objective is to evaluate the effect of clonidine on the duration of analgesia provided by a high volume-low concentration caudal block for pediatric aurgical procedres. In addition, caudal clonidine's effect on length of recovery and post-operative emergence agitation will be measured.

Eligibility

Inclusion Criteria:

  • 3 years old or less
  • Weight <= 13.3kg
  • American Society of Anesthesiology Physical Status (ASA) 1 or 2
  • Undergoing circumcision surgery
  • Patients whose plan of care includes caudal block

Exclusion Criteria:

  • Known allergy to clonidine, epinephrine, or amide local anesthetics
  • Inability or unwillingness of parent or legal guardian to give informed consent

Study details
    Circumcision

NCT04263064

Medical University of South Carolina

16 February 2024

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