Nalbuphine Versus Tramadol on Post Operative Analgesia in Abdominal Surgery on Pediatric Cancer Patient

NCT07110051 · tracked via the Priya Life Science Egypt tracker

Sponsor

National Cancer Institute, Egypt

Phase

Not applicable

Started

2025-01-15

Last updated

2025-08-11

Condition(s) studied

TramadolNalbuphineAbdominal SurgeriesPediatric Cancer

Investigational drug(s) / intervention(s)

Nalbuphine →Tramadol →

Nalbuphine: this group will a single dose of nalbuphine (0.2 mg/kg) immediately after surgery to be repeated every 8 hours for the duration of the study (72 hours)

Tramadol: this group will receive a single dose of tramadol (2 mg/kg) immediately after surgery to be repeated every 8 hours for the duration of the study (72 hours).

Study summary

In current study the investigators aim to compare between nalbuphine versus tramadol for post-operative pain control in abdominal surgeries in pediatric.

Eligibility

Sex

ALL

Min age

3 Years

Max age

12 Years

Healthy volunteers

Inclusion Criteria: * Participants will be children aged 3-12 years * American society of anesthesia (ASA) classification I-III. * scheduled for elective Abdominal surgery under general anesthesia Exclusion Criteria: * child guardian refusal. * Allergy from Tramal or nalbuphine * Patient with previous chronic pain on opioids

Primary outcome measure(s)

time to first rescue analgesia — 72 hours
Time to first analgesic request( paracetamol)

Trial sites (1)

Facility	City	Region	Status
National cancer institute	Cairo	Egypt	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07110051 on ClinicalTrials.gov ↗ ← All trials in Egypt