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To see the heart rate and blood pressure changes during start of anesthesia by giving two diffrent dose of dexmedetomidine at starting of the anesthesia

Comparison of different dose of dexmedetomidine in attenuation of hemodynamic response during Laryngoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015505
Enrollment
60
Registered
2018-08-28
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: Z409- Encounter for prophylactic surgery, unspecified Health Condition 2: Z768- Persons encountering health services in other specified circumstances

Interventions

Intervention1: Dexmedetomidine 0.5 microgram / kg: Dexmedetomidine 0.5 microgram / kg during intubation with routine induction agents TIME : For 10 minutes at the start of anesthesia Intervention2: De

Sponsors

Sri ramakrishna hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA GRADE I AND II patients Patients schedulded for elective surgery under general anesthesia Patients who provide consent for the study

Exclusion criteria

Exclusion criteria: > ASA III PATIENTS Patients with suspected difficulty in intubation resulting in more than one attempt or > 30 sec taken Patients who refused to consent for the study Patients allergic to study drug Patients who are pregnant, patient on any antidepressants, antipsychotics, patients having history of drug abuse.

Design outcomes

Primary

MeasureTime frame
Attenuation of Hemodynamic response during Laryngoscopy by safe dose of dexmedetomidine when used along with fentanylTimepoint: 1-03-2019

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactArun Muthukumar GL

Sri ramakrishna hospital

muthu74@gmail.com

Outcome results

None listed

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