to study the effect of intra peritoneal levobupivacaine on post operative pain in patients who have undergone Diagnostic laparoscopy
Not Applicable
- Conditions
- Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
- Registration Number
- CTRI/2022/11/047429
- Lead Sponsor
- rohilkhand medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)ASA risk classification1-2.
2) All women undergoing diagnostic laparoscopic surgery.
Exclusion Criteria
1)ASA >2
2) Wt <50kg due to risk of local anesthesia toxicity
3) Contra-indication or previous adverse reaction to bupivacaine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method main aim of this randomized triple blinded study was to compare post laparoscopic pain in women treated with Levobupivacaine with those treated with 0.9 <br/ ><br>% sodium chloride <br/ ><br>Timepoint: 1 year <br/ ><br>
- Secondary Outcome Measures
Name Time Method To compare the efficiency of Intraperitoneal instillation of Levobupivacaine with that <br/ ><br>of Intraperitoneal instillation of 0.9% sodium chloride in terms of: <br/ ><br>â?¢ Duration of pain relieving action <br/ ><br>â?¢ Need of post-operative analgesia <br/ ><br>â?¢ Quality of post-operative careTimepoint: 1 year