Ketodex Efficacy for adult procedural sedatio
Phase 3
Recruiting
- Conditions
- Adult procedural sedation.
- Registration Number
- IRCT20130108012072N13
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 135
Inclusion Criteria
Patients with pain severity status of Anesthesiology physical status I to III (ASA I-III),
Visual Analog Scale>4
Exclusion Criteria
?Addiction to drugs and analgesics
Use of analgesics in 24 hours ego
Underlying disease such as hypertension, liver and kidney disease)
Pregnancy
Psychiatric disease such as psychosis
Severe verbal or hearing disability
Sensitivity to Ketamine, Ketofol and Ketodex
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity score with Visual Analog Scale. Timepoint: Study beginning, 30 minutes and 1 hour and 2 hours after treatment. Method of measurement: Visual Analog Scale.;Sedation level with Ramsay Sedation Score (RASS). Timepoint: Study beginning, 30 minutes and 1 hour and 2 hours after treatment. Method of measurement: Ramsay Sedation Score (RASS).
- Secondary Outcome Measures
Name Time Method Hemodynamic changes. Timepoint: Study beginning, 30 minutes and 1 hour and 2 hours after treatment. Method of measurement: Manometer; Heart rate; Pulseoximetry.;Agitation. Timepoint: Study beginning, 30 minutes and 1 hour and 2 hours after treatment. Method of measurement: Checklist.