the Effect of intraperitoneal Bupivacaine in pain reduce
Phase 2
- Conditions
- Endometriosis.Endometriosis of uterus
- Registration Number
- IRCT20150817023666N11
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 45
Inclusion Criteria
Informed consent to enter the study
Candidate for laparoscopic surgery due to benign gynecological disease
Age between 20 and 65 years
Patients ASA I, II
women with endometriosis
Exclusion Criteria
Patients who have not signed the consent form
Patients whose laparoscopic surgery has changed to vaginal or abdominal
Patients that underwent surgery without general anesthesia
Pregnant women
Allergy to local anesthetics or Dexmedetomidine
Patients with morbid obesity
Patients with liver or kidney failure
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: before surgery and 2,4 ,6 ,12 and 24 Hour after surgery. Method of measurement: Visual analog score.
- Secondary Outcome Measures
Name Time Method