Clinical trial of analgesic Effect of intraperitoneal bupivacaine-petidine infiltration compared with intravenous paracetamol on Post gynecologic diagnostic laparoscopic pai
Phase 2
- Conditions
- Change in pain after laparoscopy.
- Registration Number
- IRCT2013072810765N4
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
Women with 20-38 years old; candidated for gynecologic diagnostic Laparoscopy; patients with ASA physical status I and II; patients who will give written informed consent
Exclusion criteria: Women with ASA physical status III or higher;patients who received analgesic; patients who had contraindication for NSAIDs or Paracetamol like peptic ulcer; coagulopathy; renal failure;hepatic failure; allergy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: 2, 4, 6, 8, 12, 24 hours postoperative. Method of measurement: with the use of visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Sedation. Timepoint: 2, 4, 6, 8, 12, 24 hours post operative. Method of measurement: with the use of modified Ramssy sedation scoring.