None listed
Conditions
Interventions
Intervention1: Group 2C: All patients in this group will receive bilateral USG guided Tranversus Abdominis Plane Block with twenty milliliter of 0.2% Ropivacaine combined with Butorphanol 0.5 milligra
Sponsors
North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients belonging to ASA class I and class II. 2. Patients scheduled for elective laparoscopic cholecystectomy. 3. Patients who understand Visual Analogue Scale(VAS)
Exclusion criteria
Exclusion criteria: 1. History of allergy to local anesthetics 2. History of opoid addiction. 3. History of coagulopathy. 4. Infection at the site of needle entry. 5. Recent intake of alcohol/ sedatives/ analgesic/ narcotics. 6. History of co- morbid diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the quality and duration of post operative analgesia by adding butorphanol(opoid) to ropivacaine (local anesthetic) in USG guided tranversus abdominis plane block.Timepoint: To assess the quality of post operative pain immediately after the block then, every thirty minutes for next three hours then every three hours for twenty fours. | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the sadation score using Modified Ramsay Sedation Scale, Pulse rate, Systolic blood pressure, Diastolic blood pressure, Mean blood pressure, Respiratory rate and Side effects, if any.Timepoint: Assessment will be done immediately after the block then, every thirty minutes for three hours then every three hourly for twenty four hours. | — |
Countries
India
Contacts
Public ContactDr Rajani Thabah
North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences
Outcome results
None listed