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Effect of preoperative infusion of dexmedetomidine on intraoperative anaesthetic drug consumption under general anaesthesia

Effect of preanaesthetic single infusion of dexmedetomidine on isoflurane consumption in surgical patients under general anaesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/026088
Enrollment
100
Registered
2020-06-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patient with American Society of Anaesthesiologists Physical status 1 and 2 posted for elective surgery under general anaesthesia

Interventions

Intervention1: normal saline: placebo Intervention2: preanaesthetic single infusion of dexmedetomidine: dexmedetomidine - alpha 2 agonist, used as sedation Intervention3: Intravenous infusion: single

Sponsors

M S RAMAIAH MEDICAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Age between 20 and 60 years. - American Society of Anaesthesiologists Grade 1 and 2. - Patients undergoing surgeries under general anaesthesia.

Exclusion criteria

Exclusion criteria: - Patients allergic to study drug. - Patients undergoing laparoscopic surgeries. - Body Mass Index > 35 kg/m2. - Patients on beta blockers,sedatives or stimulant drugs. -Patients with history of psychiatric illness,alcohol abusers,altered mentation or epilepsy.

Design outcomes

Primary

MeasureTime frame
To assess the effect of preanaesthetic administration of dexmedetomidine on isoflurane consumption.Timepoint: At the end of the surgery

Secondary

MeasureTime frame
To assess effect of dexmedetomidine on intraoperative haemodynamic stability and recovery profile.Timepoint: Baseline,every 5 minutes after infusion of study drug/placebo till end of anaesthesia heart rate,blood pressure,oxygen saturation,bispectral index values were noted. Postoperative recovery profiles were assessed using modified aldrete score at immediate postop,30 and 60 minutes.

Countries

India

Contacts

Public ContactRESHMA B M

M.S.RAMAIAH MEDICAL COLLEGE

jageedha@yahoo.com9900482828

Outcome results

None listed

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