The effect of vitamin C on agitation induced by naltrexone, a randomized clinical trial study
Phase 1
- Conditions
- agitation.agitation
- Registration Number
- IRCT201107046948N1
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 31
Inclusion Criteria
Patients between ages 18-40; opioid abusers; coming to the hospital with withdrawal symptoms including agitation; caused by misusing of naltrexone. Exclusion criteria: Patients who had an underlying medical disorder (diabetic mellitus, renal failure, cardiovascular disease, renal stone and those undergo dialysis); pregnant women; those who were very agitated and need intubation.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Agitation. Timepoint: every one hour. Method of measurement: RAAS score.
- Secondary Outcome Measures
Name Time Method Rhabdomyolysis. Timepoint: after first 24 hours. Method of measurement: urine analysis.