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BIS monitoring in Dexmedetomidine infusion during laproscopic surgeries to reduce sevoflurane requirement

A prospective randomised controlled study utilising Bispecrtal index guidance to investigate the impact of Dexmedetomidine on Sevoflurane consumption during elective laproscopic surgeries. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092194
Enrollment
60
Registered
2025-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: effect of Dexmedetomidine infusion in laproscopic surgeries: To study the effect of Dexmedetomidine on sevoflurane consumption using BIS monitoring in laproscopic surgeries Control Inte

Sponsors

Vinayaka Missions Kirupananda Variyar Medical College and Hospitals Chinnaseeragapadi Salem
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of Dexmedetomidine on sevoflurane requirements during elective laproscopic surgeriesTimepoint: From 0 minutes of dexmedetomidine infusion till the end of procedure

Secondary

MeasureTime frame
Assessment of the hemodynamic parameters and thereby enabling the titration of the anesthetic agent based on BIS monitoringTimepoint: From 0 min of administration to 90 mins post administration

Countries

India

Contacts

Public ContactDr Harshini T

Vinayaka Missions Kirupananda Variyar Medical College and Hospitals Chinnaseeragapadi Salem

naveenasen@gmail.com6382660052

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026