Effect of propofol-ketamine and propofol-sufentanil on sedation and analgesia in painful diagnostic methods in children with hematological malignancies
Phase 2
- Conditions
- Acute lymphoblastic leukaemia [ALL].Acute lymphoblastic leukemia [ALL]
- Registration Number
- IRCT20170809035601N9
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Children aged 1 to 14 years
Hematologic malignancies
Acute lymphoblastic leukemia
Exclusion Criteria
A recent trauma to the head
Cardiovascular, pulmonary, or liver diseases
Epilepsy, seizure or neurological disorder
Use of analgesic or sedative medications before surgery
Chronic pain syndrome
History of allergy to the drugs studied
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation level. Timepoint: During procedure. Method of measurement: university of michigan sedation scale.
- Secondary Outcome Measures
Name Time Method Analgesia. Timepoint: During procedure. Method of measurement: Universal Pain Assessment Tool.