Comparison of analgesia with two groups of drugs for inguinal hernia repair surgeries.
Phase 4
Completed
- Conditions
- Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangrene
- Registration Number
- CTRI/2018/03/012725
- Lead Sponsor
- VIJAYALAKSHMI SIVAPURAP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ALL AMERICAN SOCIETY OF ANAESTHESIOLOGISTS CLASS I & II PATIENTS UNDERGOING UNILATERAL INGUINAL HERNIA REPAIR SURGERIES UNDER SPINAL ANESTHESIA
Exclusion Criteria
ANY PATIENT NOT WILLING TO ENROLL OR PATIENTS WITH ALLERGY TO BUPIVACAINE, CLONIDINE, TRAMADO
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the total duration of rescue analgesia(time to rescue analgesia, i.e. first request for analgesia)Timepoint: To compare the total duration of rescue analgesia(time to rescue analgesia, i.e. first request for analgesia by patient)
- Secondary Outcome Measures
Name Time Method TO COMPARE 24 HOUR ANALGESIC REQUIREMENT IN MG/KGTimepoint: FOR 24 HOURS;TO COMPARE HEART RATE, BLOOD PRESSURE SPO2 POSTOPERATIVELYTimepoint: EVERY 15 MINUTES FOR FIRST 2 HOURS;TO COMPARE PROPORTION OF SIDE EFFECTS IF ANYTimepoint: FOR 24 HOURS;TO COMPARE VAS SCORESTimepoint: AT 2, 4, 6, 12 AND 24 HOURS POSTOPERATIVELY