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A comparison of intranasal dexmedetomidine versus placebo in attenuation of hemodynamic responses to laryngoscopy and intubation

A randomized double-blind controlled study of attenuation of hemodynamic responses to laryngoscopy and intubation after intranasal administration of dexmedetomidine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044460
Enrollment
166
Registered
2022-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Dexmedetomidine: Intranasal administration of dexmedetomidine at a dose of 1 micrograms/kg body weight 45 minutes prior to induction Control Intervention1: 0.9 % normal saline: Intrana

Sponsors

Kidwai memorial institute of oncology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18 to 65 years belonging to ASA status 1 ad 2 with BMI between 18 -25 kgm2 undergoing surgery under general anesthesia

Exclusion criteria

Exclusion criteria: Patient refusal. Patient with known nasal pathology. History of allergy to study drug or other anesthetic agents.patient with history ischemic heart disease, cerebrovascular accident, or cardiovascular disease. Patient with second or third degree heart blocks. Patients on long term sedatives or anxiolytics. Patients on Anti hypertensive like clonidine, beta blockers, alpha methyl dopa, alpha adrenergic agonists.

Design outcomes

Primary

MeasureTime frame
Hemodynamic responses to laryngoscopy and intubationTimepoint: 60 minutes

Secondary

MeasureTime frame
Sedation, anxioysisTimepoint: 45 minutes

Countries

India

Contacts

Public ContactDr Namrata Ranganath

Kidwai memorial institute of oncology

namrang@gmail.com919880642830

Outcome results

None listed

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