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Comparative study of morphine, fentanyl or nalbuphine patient controlled analgesia for mucositis pain in pediatric patients undergoing cancer therapy: A randomized clinical trial

Comparative study of morphine, fentanyl or nalbuphine patient controlled analgesia for mucositis pain in pediatric patients undergoing cancer therapy: A randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
PACTR
Registry ID
PACTR202403689052671
Enrollment
90
Registered
2024-03-28
Start date
2018-09-15
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Anaesthesia

Interventions

Sponsors

Childrens Cancer Hospital Egypt 57357
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: both sexes aged 7-18 years admitted to the Children Cancer Hospital Egypt 57357 diagnosed with cancer and undergoing cancer therapy complicated by mucositis grade 3 and 4 (severe oral mucositis)

Exclusion criteria

Exclusion criteria: central nervous system disorders, delayed developmental milestones, or mental retardation that might interfere with the assessment of pain intensity known or suspected myopathy known or suspected allergy to any narcotic known history of intolerable side effects of opioids renal impairment (creatinine clearance less than 50 mL/min) hepatic dysfunction (liver enzymes elevated more than 10-fold) respiratory distress (SPO2 less than 92% on room air) cardiac disease (ejection fraction less than 40%) chronic pain complaints advanced or metastatic cancer scheduled for palliative care

Design outcomes

Primary

MeasureTime frame
Pain intensity using the Visual Analog Scale;Number of active and total pushes of PCA buttons;Total opioid consumption;Patient satisfaction using the Patient Satisfaction Score

Secondary

MeasureTime frame
Adverse effects e.g. sedation, respiratory depression, bradycardia, hypotension, nausea, vomiting, pruritus, and urine retention.

Countries

Egypt

Contacts

Public ContactAhmed Ibrahim

Department of Anesthesia Intensive Care and Pain Management Faculty of Medicine Ain Shams University

ahmed.ibrahim@email.com00000000000000

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026