Effect of Ketamine for pediatrics pai
- Conditions
- pain during Intravenous placement in pediatrics.
- Registration Number
- IRCT201504251764N3
- Lead Sponsor
- Vice chancellor for research,Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
children with no pain at baseline will enter the study? also children take part in the study who are able to take the drug orally.
Exclusion criteria: having any medical condition in which procedure is emergent and there is no 20-30 minutes chance to take analgesic; having any contraindication for prescribing ketamine (included but not limited to high blood pressure; high intracranial pressure; high intraocular pressure; Heart failure; Thyroid diseases; Respiratory system instability); the history of taking ketamine by patient in the last 24 hour in this center (in this study); 4. American Society of Anesthesiologists class= III; abnormal neurological exam; lack of parental consent; having any condition that makes evaluating pain difficult; Glasgow Coma Scale less than 15.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain while Intravenous placement in pediatrics. Timepoint: 30 minutes after taking oral Ketamine. Method of measurement: Measurement of pain in children ; pain score(Children's Hospital of Eastern Ontario Pain Scale, Visual Analog Scale).;Cooperation during catheter insertion. Timepoint: 30 minutes after taking the oral ketamine. Method of measurement: I.V Sedation Scale.
- Secondary Outcome Measures
Name Time Method Potential side effects due to use of oral ketamine. Timepoint: first 1 hour and 24 hours after taking of oral ketamine. Method of measurement: Checklist of side effects of ketamine.