CTRI/2025/08/092194
Not yet recruiting
Phase 3
A prospective randomised controlled study utilising Bispecrtal index guidance to investigate the impact of Dexmedetomidine on Sevoflurane consumption during elective laproscopic surgeries.
Vinayaka Missions Kirupananda Variyar Medical College and Hospitals Chinnaseeragapadi Salem1 site in 1 country60 target enrollmentStarted: August 13, 2025Last updated:
Overview
- Phase
- Phase 3
- Status
- Not yet recruiting
- Sponsor
- Vinayaka Missions Kirupananda Variyar Medical College and Hospitals Chinnaseeragapadi Salem
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- To evaluate the effect of Dexmedetomidine on sevoflurane requirements during elective laproscopic surgeries
Overview
Brief Summary
This is a randomised controlled trial to help in evaluating the effect of dexmedetomidine infusion on sevoflurane requirement using BIS monitoring in patients undergoing elective laparoscopic procedures.
Study Design
- Study Type
- Interventional
- Allocation
- Other
- Masking
- Participant Blinded
Eligibility Criteria
- Ages
- 20.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •patient giving valid informed consent ASA 1 and ASA 2 MP 1 and MP2 Elective laproscopic surgeries BMI- 18.5 TO 24.9.
Exclusion Criteria
- •patient refusal ASA 3 and ASA 4 Age less than 20 and above 65 patient with ischemic and rheumatic heart disease patients on alpha agonist, antagonist and beta blockers allergies to medications.
Outcomes
Primary Outcomes
To evaluate the effect of Dexmedetomidine on sevoflurane requirements during elective laproscopic surgeries
Time Frame: From 0 minutes of dexmedetomidine infusion till the end of procedure
Secondary Outcomes
- Assessment of the hemodynamic parameters and thereby enabling the titration of the anesthetic agent based on BIS monitoring(From 0 min of administration to 90 mins post administration)
Investigators
Dr Arun Kumar
Vinayaka Missions Kirupananda Variyar Medical College and Hospitals Chinnaseeragapadi Salem
Study Sites (1)
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