The effect of Ondansetron on pain caused by Etomidate injectio
Phase 3
Recruiting
- Conditions
- Pain caused by Etomidate.
- Registration Number
- IRCT20160307026950N38
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients 18 to 60 years
Grade I and II in ASA criteria (American Society of Anesthesia)
Candidate for general anesthesia with Etomidate
Exclusion Criteria
Patients with Heart Disease
Patients with Psychologic disease
Allergic to drugs used in the study
Taking sedatives or painkillers 24 hours before anesthesia
Addiction to drugs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of pain caused by Etomidate injection. Timepoint: During the injection until 30 seconds. Method of measurement: Faces Pain Rating Scale (FPRS).
- Secondary Outcome Measures
Name Time Method Heart Rate. Timepoint: Before injection, immediately after injection, 5 and 10 minutes after Etomidate injection and then every 15 minutes until the end of the operation. Method of measurement: ECG monitoring.;Moderate arterial blood pressure. Timepoint: Before injection, immediately after injection, 5 and 10 minutes after Etomidate injection and then every 15 minutes until the end of the operation. Method of measurement: Barometer.;Arterial blood oxygen saturation. Timepoint: Before injection, immediately after injection, 5 and 10 minutes after Etomidate injection and then every 15 minutes until the end of the operation. Method of measurement: Pulse oximeter.;Duration of anesthesia. Timepoint: From the beginning of anesthesia to the end of recovery. Method of measurement: Clock.