CTRI/2024/11/076980Not yet recruitingPhase 4
Comparison of Post Operative Analgesic Efficacy of Bupivacaine and Ropivacaine with Dexmedetomidine using Ultrasound Guided Subcostal Transverse Abdominis Plane Block in Laparoscopic Cholecystectomy under General Anaesthesia
Gandharv Singh1 site in 1 country60 target enrollmentStarted: December 1, 2024Last updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- To study and compare Post Operative Analgesic Efficacy of Bupivacaine and Ropivacaine with Dexmedetomidine using Ultrasound Guided Oblique Subcostal Transverse Abdominis Plane Block in Laparoscopic Cholecystectomy under General Anaesthesia
Study Overview
Brief Summary
Using ultrasound guided subcostal transverse abdominis plane block, for post operative pain relief, for patients undergoing laparoscopic cholecystectomy, efficacy of bupivacaine with dexmedetomidine will be compared with ropivacaine with dexmedetomidine, through follow up of patients post operatively, for pain scoring.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Participant and Investigator Blinded
Eligibility Criteria
- Ages
- 20.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Male and Female between Age group 20- 60 years.
- •ASA I-II BMI 18.5-29.
- •Patient giving consent.
Exclusion Criteria
- •Patient’s refusal to participate in the study.
- •Patients having bleeding disorders.
- •Hypersensitivity to local anaesthetics and study drugs.
- •Local infection at the site where needle is to be inserted.
- •Patients with dysrhythmias, and on beta blockers.
- •Patients on anticoagulants.
Outcomes
Primary Outcomes
To study and compare Post Operative Analgesic Efficacy of Bupivacaine and Ropivacaine with Dexmedetomidine using Ultrasound Guided Oblique Subcostal Transverse Abdominis Plane Block in Laparoscopic Cholecystectomy under General Anaesthesia
Time Frame: 1 hour, 4 hours, 8 hours, 12 hours, 24 hours
Secondary Outcomes
- 1. To study total top up analgesic doses requirement in 24 hours post operatively.(2. To study for side effects if any.)
Investigators
Gandharv Singh
Dr Rajendra Prasad Government Medical College Tanda Kangra Himachal Pradesh
Study Sites (1)
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