Comparison Intraperitoneal Ropivacaine alone and with Dexmedetomidin and Fentanyl on pain management in abdominal laparoscopic
Phase 2
Recruiting
- Conditions
- abdominal elective laparoscopic.
- Registration Number
- IRCT20141209020258N117
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 138
Inclusion Criteria
Patients candidate laparoscopic abdominal surgery
18 to 65 years old
No susceptibility to used drugs
Absence of cardiovascular disease and endocrine and renal disease
No smoking and no addiction
No pregnancy
Body mass index more than 35
Exclusion Criteria
No willingness to continue the study
Refusal of the patient to inject intraperitoneally
Patient that requires the insertion of a drain inside the abdomen for any reason
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean arterial blood pressure. Timepoint: Every 30 minutes during surgery and recovery and 2 hours after surgery. Method of measurement: Barometer.;Heart rate. Timepoint: Every 30 minutes during surgery and recovery and 2 hours after surgery. Method of measurement: Count.;Percent of oxygen saturation. Timepoint: Every 30 minutes during surgery and recovery and 2 hours after surgery. Method of measurement: Pulse oximetry.;Pain. Timepoint: At recovery and 2, 4, 6, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale Questionnaire.;Amount of opioids consumed during surgery. Timepoint: End of surgery. Method of measurement: Milligram.
- Secondary Outcome Measures
Name Time Method