The effect of Valsalva maneuver and tourniquet closure on Propofol injection pai
Phase 3
Recruiting
- Conditions
- Pain from propofol injection.Pain, not elsewhere classified
- Registration Number
- IRCT20160307026950N28
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 105
Inclusion Criteria
Age 18 to 65 years
ASA class I and II
candidate for surgery under the general anesthesia
Able to perform Valsalva maneuver
Exclusion Criteria
Having respiratory problems
Drug addiction and stimulants
Allergy to Propofol
Having underlying diseases such as diabetes, cardiovascular problems, liver disorders
Existence of chronic pain syndromes and thrombophlebitis
Take any analgesic and sedative before anesthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain from propofol injection. Timepoint: 20 seconds after propofol injection. Method of measurement: withdrawal response score questionnaire.
- Secondary Outcome Measures
Name Time Method Blood Pressure. Timepoint: Before intervention, after intervention, after injection of propofol every 1 to 3 minutes, 5 minutes after induction of anesthesia, 10 minutes after induction of anesthesia. Method of measurement: Barometer.;Heart Rate. Timepoint: Before intervention, after intervention, after injection of propofol every 1 to 3 minutes, 5 minutes after induction of anesthesia, 10 minutes after induction of anesthesia. Method of measurement: ECG monitoring.;Arterial blood oxygen saturation. Timepoint: Before intervention, after intervention, after injection of propofol every 1 to 3 minutes, 5 minutes after induction of anesthesia, 10 minutes after induction of anesthesia. Method of measurement: Pulse Oximeter.