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Reduction of response during visualisation of throat and passing a tube through the wind pipe with a different injection

Attenuation of haemodynamic responses to laryngoscopy and intubation with intravenous dexmedetomidine: A randomised controlled trial on comparison between two doses.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/050146
Enrollment
90
Registered
2023-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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: Dexmedetomidine: Dexmedetomidine is an α-2 agonist which has property of good anxiolysis, sedation and analgesic action.This study compares different doses of dexmedetomidine -0.5 mcg

Sponsors

Anna Mary George
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) Physical Status 1 and 2 Age 18 â??59 years Posted for elective surgeries under general anaesthesia

Exclusion criteria

Exclusion criteria: Patients who are physically dependent on narcotics Those with a history of bronchial asthma, drug or alcohol abuse. Known drug allergy to either clonidine or dexmedetomidine, Cerebrovascular, neurologic, respiratory or ischemic heart disease (history of angina, previous myocardial infarction) Renal and hepatic dysfunction. Patients on alpha-blockers, antidepressants, anxiolytics, anticonvulsant or antipsychotics Any predicted difficult airway

Design outcomes

Primary

MeasureTime frame
To arrive at an optimal dose of IV dexmedetomidine by comparing different doses of the drug with normal saline in terms of attenuation of haemodynamic stress response to laryngoscopy and endotracheal intubationTimepoint: Recorded at 1, 3 , 5 and 10 min after intubation

Secondary

MeasureTime frame
To assess the sedation after the drug infusion based on Ramsay sedation score.Timepoint: Recorded at 1, 3 , 5 and 10 min after intubation

Countries

India

Contacts

Public ContactAnna Mary George

ST JOHNS MEDICAL COLLEGE,BANGALORE

sathyanarayananair@yahoo.com9448066128

Outcome results

None listed

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