A clinical trial to evaluate the instillation of lignocaine during laparoscopc tubal ligation as a pain relief measure during and after surgery
Phase 3
Completed
- Registration Number
- CTRI/2009/091/000072
- Lead Sponsor
- Kasturba Medical College, Manipal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
All women who desired laparoscopic sterilization under local analgesia and sedation were included in the study
Exclusion Criteria
known hypersensitivity to local anesthetics, history of seizures or known cardiac or renal disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score was measured using visual analogue scale (VAS)Timepoint: Pain score measured intra operatively during manipulation of tubes and Falope ring application and post operatively at 0.5 hours, one hour and three hours.
- Secondary Outcome Measures
Name Time Method Post operative nausea, vomiting and any symptoms of lignocaine toxicity were also recordedTimepoint: 6 hours