Nebulized Bupivacaine Analgesia for Cleft Palate Repair

Status Recruiting

Clinical Trial Summary

In this study we introduce a potent local anesthetic; bupivacaine 0.5% in two different doses by nebulization as a preemptive analgesia to compare efficacy and safety in children with cleft palate repair.

Clinical Trial Description

A written informed consent will be taken from the guardian of children. Patients will be assigned randomly to three groups (30 subjects each) to be anesthetized. The study drug will be delivered in opaque bags labeled "study drug" and 90 patients will be allocated in three groups (of 30 patients each) to receive; Nebulized Bupivacaine 0.50% 0.25 mg.kg-1 (Group B1) or Nebulized Bupivacaine 0.50% 0.50 mg.kg-1 (Group B2) or same volume of saline placebo (Group C). ;

Study Design

Related Conditions & MeSH terms

Cleft Palate

Clinical Trial Details

NCT number	NCT04928352
Study type	Interventional
Source	Assiut University
Contact	Omar Soliman, MD
Phone	01101266040
Email	omarmakram347@yahoo.com
Status	Recruiting
Phase	Phase 3
Start date	June 14, 2021
Completion date	June 20, 2024

View Details

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