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Efficacy of addition of dexmedetomidine/clonidine to fentanyl to blunt Pressor Response of Laryngoscopy and Intubation

An evaluation of efficacy of addition of dexmedetomidine/clonidine to fentanyl in Attenuation of Pressor Response of Laryngoscopy and Intubation : A prospective double blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/03/012549
Enrollment
96
Registered
2018-03-13
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- healthy of ASA grade I &II

Interventions

None listed

Sponsors

RNT Medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Scheduled for elective surgeries under general anaesthesia 2)ASA grade I and II

Exclusion criteria

Exclusion criteria: 1)Baseline heart rate less than 60 per minute 2)Baseline blood pressure less than 100/50 mm of hg 3)Reactive airway disease 4)History of cardiac disease and hypertensive patient 5)Requiring 2 or more attempts for laryngoscopy and intubation will be excluded from the study

Design outcomes

Primary

MeasureTime frame
An evaluation of efficacy of addition of dexmedetomidine/clonidine to fentanyl in Attenuation of Pressor Response of Laryngoscopy and Intubation : A prospective double blind randomized controlled trialTimepoint: 1 year—

Secondary

MeasureTime frame
AwaitedTimepoint: Awaited—

Countries

India

Contacts

Public ContactDr Rekha meena

rnt medical college udaipur

drlalitkumar@hotmail.com9414352823

Outcome results

None listed

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