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Comparing two doses of dexmedetomidine for decreasing the response to tube placement in patients undergoing surgeries

Comparison of Two Different Doses of Intravenous Dexmedetomidine to Attenuate Hemodynamic Responses to Direct Laryngoscopy and Intubation in Adult Patients Undergoing Elective Surgeries under General Anaesthesia - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/03/064847
Enrollment
30
Registered
2024-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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: nil: nil

Sponsors

DR SHIVAKUMAR G
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who are willing to give consent. 2.Patients of both sexes aged 18-60 years. 3.American society of Anaesthesiologist (ASA) I and II Physical status. 4.Modified Mallampati Grade 0/I/II.

Exclusion criteria

Exclusion criteria: 1.Patients with anticipated difficult airway. 2. Patients with ischemic heart disease, hypertension, and diabetes. 3.Body mass index more than 30.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of two different doses of dexmedetomidine (0.5mcg/kg and 0.75mcg/kg) for attenuation of hemodynamic response to laryngoscopy and endotracheal intubation in adult patients undergoing elective surgeries under general anaesthesia.Timepoint: 1min,2min,3min,5min,10min—

Secondary

MeasureTime frame
To determine dose dependent side effects like hypotension, bradycardia and sedation between two different dosesTimepoint: 1min,2min,3min,5min,10min—

Countries

India

Contacts

Public ContactDR SHIVAKUMAR G

mandya institute of medical sciences

dranashiv@gmail.com9900468451

Outcome results

None listed

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