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Caudal Dexamethasone - Bupivacaine in Neonates

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07609836
Enrollment
150
Registered
2026-05-27
Start date
2026-05-01
Completion date
2026-12-01
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

We Are Studying the Effects of Caudal Dexamethasone in Neonates Undergoing Inguinal Hernia Repair

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

Interventions

PROCEDUREWe add Dexamethasone to Bupivacaine as adjuvant to Bupivacaine in neonsates undergoing inguinal hernia repair in Dexamethasone - Bupivacaine group

We add Dexamethasone to Bupivacaine as adjuvant to Bupivacaine in neonates undergoing inguinal hernia repair

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Days to 28 Days
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

Design outcomes

Primary

MeasureTime frameDescription
FLACC pain scale (face,leg , activity,cry, consolability) in the first 24 hours postoperative6 monthsAssessment for additive analgesic effects of caudal Dexamethasone

Contacts

CONTACTSawsan Haridy Ahmed Abu El Hassan, Lecturer of anesthesia
sawsan_haridy@med.asu.edu.eg002- 01228118341

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026