Comparison of nerves block in female patients
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/06/053597
- Lead Sponsor
- T Revanth Prasad
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age between 18 and 5O years
2.American society of Anesthesiologists [ASA]
physical status I to III
3.Body mass index between 18 and 35 kg/m2
4.Undergoing gyanecological [fibroid/endometriosis]
laparoscopic surgery
Exclusion Criteria
1.Inability to consent to the study
2.Coagulopathy
3.Sepsis
4.Hepatic or Renal failure
5.Allergy to local anesthetic [LA]
6.Opioid intake at home
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of recovery assessed using the Quality of recovery-15 [QoR-15] scaleTimepoint: All parameters will be recorded 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method 1.Static [at rest] & dynamic <br/ ><br> [with movement] pain scores <br/ ><br> and [Numeric rating scale <br/ ><br> score 1-10] <br/ ><br>2.Performance time <br/ ><br> [the temporal interval <br/ ><br> between the start of skin <br/ ><br> disinfection and the end of <br/ ><br> Local anesthetic injection <br/ ><br> through the block needle] <br/ ><br>3.The block related adverse <br/ ><br> events [ vascular puncture, <br/ ><br> paresthesia,local anesthetic <br/ ><br> toxicity] <br/ ><br> <br/ ><br>Timepoint: All parameters recorded post operatively at 3,6,12,24 hours