A study to see the safety and efficiency of low dose spinal anaesthesia in daycare female sterilization procedures
Not Applicable
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2019/03/017929
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I and II
SURGERY- ELECTIVE LAPAROSCOPIC TUBAL LIGATIO
Exclusion Criteria
patient refusal
any contraindication to spinal anaesthesia
allergy to any of the study drugs
BMI >35
ASA III and IV
h/o any chronic abdominopelvic painful conditions
patients already on longterm opioids or non opioid analgesics
inability to comprehend VAS pain assessment scale
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method OVERALL PATIENT COMFORT DURING THE PROCEDURE <br/ ><br>PATIENT VAS RATING DURING THE PROCEDURETimepoint: OVERALL PATIENT COMFORT DURING THE PROCEDURE & OVERALL <br/ ><br>PATIENT VAS RATING DURING THE PROCEDURE BOTH TO BE ASSESSED AT THE END OF THE PROCEDURE
- Secondary Outcome Measures
Name Time Method impact on discharge criteria- <br/ ><br>-time to oral intake <br/ ><br>-time to void <br/ ><br>-time to ambulate <br/ ><br>incidence of adverse eventsTimepoint: after the procedure every half hourly for 4 hours and over phone thrice on the next day and twice the day after.