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Use of Intravenous Paracetamol in Combination with Morphine in sickle cell disease children with vaso-occlusive crisis

Efficacy of intravenous paracetamol in combination with opiod infusion for sickle cell disease children in vaso-occlusive crisis: a single-blinded randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN34491330
Enrollment
200
Registered
2009-10-26
Start date
2008-05-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Sickle cell disease with vaso-occlusive crisis Haematological Disorders Sickle-cell disorders

Interventions

Use of IV paracetamol in combination with morphine versus use of placebo with morphine: Group A (standard treatment): morphine (weight of the child multiplied by constant 0.5 = *mg of morphine) and pl
no standard period. The period of hospital stay will be compared later to see if there is any reduction by adding IV paracetamol to morphine treatment. The patient will have liver function tests perfo

Sponsors

Sultan Qaboos University (Oman) - College of Medicine and Health Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All sickle cell disease (SCD) children (aged 2 - 13 years, either sex) admitted with vaso-occlusive crisis (VOC) in B2 (blue two) ward of Sultan Qaboos University Hospital (SQUH)

Exclusion criteria

Exclusion criteria: 1. Children aged less than one year 2. Children with fever of more than 38.5°C 3. Children with prior side effects of morphine 4. Children with prior history of side effects of paracetamol 5. Children with severe jaundice or severe liver impairment

Design outcomes

Primary

MeasureTime frame
Reduction in the amount of morphine and duration of hospitalisation, assessed on a daily basis.

Secondary

MeasureTime frame
Assessed on a daily basis: 1. Reduction in duration of hospital stay (days) for pain relief 2. Reduction in pain severity on a scale of 1 - 10, which will be assessed each shift 3. Reduction of morphine requirements 4. Reduction in morphine side effects namely: prurities, nausea/vomiting, urinary retention

Countries

Oman

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026