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Clinical Trials/NCT07609836
NCT07609836Not yet recruitingNot Applicable

Analgesic Efficacy Of Dexamethasone As Adjuvant To Caudal Bupivacaine For Neonates Undergoing Inguinal Hernia Repair: Randomized Controlled Study

Ain Shams University0 sites150 target enrollmentStarted: May 1, 2026Last updated:
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Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
150
Study OverviewStudy DesignEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Randomied controlled study Evaluate the effects of caudal Dexamethasone in neonates

Detailed Description

Evaluate the additive analgesic effects of caudal Dexamethasone in neonates undergoing inguinal hernia repair.

additive side effects if found

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
1 Day to 28 Days (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •full term neonate
  • •ASA I & ASA II
  • •Scheduled for inguinal hernia repair

Exclusion Criteria

  • •Patients with allergies to studied drugs
  • •body weight <3 kilograms
  • •parents refusal

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

sawsan haridy ahmed aboelhassan

Lecturer and Consultant of Anesthesiology in Ain Shams University.

Ain Shams University

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