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sedation in children with hematology cancer

The Incidence and Nature of Adverse Events during Paediatric Sedation and analgesia: A randomized crossover controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201403000762218
Enrollment
60
Registered
2014-02-06
Start date
2014-01-06
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Surgery Paediatrics cancer Anaesthesia

Interventions

ketofol (1:1 mixture of propofol and ketamine)
MK group

Sponsors

ADEKOLA LATEEF
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ASA I-II children aged 1-15 years undergoing procedural sedation and analgesia for haematological malignancy All consecutive children with haematological cancer undergoing bone marrow aspiration/biopsy and lumbar puncture (LP) for chemotherapy in the paediatric oncology ward

Exclusion criteria

Exclusion criteria: prior sensitization or allergic reaction to propofol, ketamine, soy or egg products presences of hypotension, head injury, increased intracranial increased intraocular pressure use of drugs known to interact with any of the study agent patients who have been involved in another study in the last 30 days. Patients with heart, lung or neurological disease, and central nervous system disorders symptomatic thrombocytopenia, age less than 1 year or over 15 years ASA IV-V patients

Design outcomes

Primary

MeasureTime frame
1.A change less than or greater than 20% change in Heart Rate 2.A change less than or greater than 20% in Respiratory Rate 3.Systolic blood pressure greater than the fifth percentile of normal for age 4.Systolic blood pressure less than the fifth percentile of normal for age 5.Movement during sedation

Secondary

MeasureTime frame
1. To determine if spontaneous ventilation continues following administration of the anaesthetic agents for sedation. 2. Pain (Yes/No), the participant will be monitored from the end of the procedure until sedation recovery

Countries

Nigeria

Contacts

Public ContactE Temiye

Professor of Paediatric Oncology/ Lagos University Teaching Hospital

emtemiye@unikag.edu.ng+2348023123902

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026