CTRI/2022/10/046296Not yet recruitingPhase 4
Regional nerve blocks in adjunct to general anaesthesia versus general anaesthesia alone for faciomaxillary surgeries-a randomised controlled study
Dr Nithyashree Singh1 site in 1 country70 target enrollmentStarted: October 13, 2022Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 70
- Locations
- 1
- Primary Endpoint
- To compare the intraoperative analgesic effect of regional nerve blocks upto 24hours after block
Study Overview
Brief Summary
We compare the intraoperative and postoperative analgesia in two groups where one group receives regional nerve blocks and general anaesthesia while other group receives only general anaesthesia for faciomaxillary surgeries.
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Participant and Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •patients willing to give written consent 2) patients aged 18-60years of both genders 3) patients scheduled for elective faciomaxillary surgeries under general anaesthesia 4) ASA I and ASA II patients.
Exclusion Criteria
- •patients with ASA 3 and ASA 4 2) Pregnant women 3) patients with known allergy to study drug.
Outcomes
Primary Outcomes
To compare the intraoperative analgesic effect of regional nerve blocks upto 24hours after block
Time Frame: Time of rescue analgesia postoperatively upto 24hours
Requirement of rescue analgesia postoperatively
Time Frame: Time of rescue analgesia postoperatively upto 24hours
Secondary Outcomes
- To minimise the side effects of postoperative opioids(6th hour , 12th hour and 24hours after surgery)
Investigators
Study Sites (1)
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