The effect of intravenous and intraperitoneal dexmedetomidine in combination with intraperitoneal bupivacaine on postoperative pai
Phase 3
Recruiting
- Conditions
- postoperative pain.
- Registration Number
- IRCT20160307026950N53
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Candidates for laparoscopic cholecystectomy surgery
ASA I & II(American society of anesthesiologist)
Informed Consent to participate in the study
Exclusion Criteria
Patients with a history of allergy to the drugs used in the study (dexmedetomidine and bupivacaine)
Patients with psychological problems
Patients with a history of drug addiction
Patients with the inability to express the intensity of pain based on the vas criterion
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The severity of postoperative pain. Timepoint: In base time9before intervention), every 15 minutes in recovery,in 2, 4, 6, 12, 24 hours after surgery. Method of measurement: Visual Analogue Scale(0-10).
- Secondary Outcome Measures
Name Time Method Heart Rate. Timepoint: In base time(before intervention), every 30 minutes during operation and then in recovery. Method of measurement: ECG.;Arterial blood oxygen saturation. Timepoint: In base time(before intervention), every 30 minutes during operation and then in recovery. Method of measurement: pulse oximeter.;Complication(nausea and vomiting). Timepoint: In base time(before intervention), every 30 minutes during operation and then in recovery. Method of measurement: asking.;Mean arterial pressure. Timepoint: In base time(before intervention), every 30 minutes during operation and then in recovery. Method of measurement: barometer.