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A study to compare how well intravenous dexmedetomidine and intravenous preservative free lignocaine reduces changes in blood pressure and heart rate during administration of general administration with endotracheal tube

A study to compare intravenous dexmedetomodine with intravenous preservative free lignocaine for attenuation of hemodynamic responses to laryngoscopy and endotracheal intubation - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080067
Enrollment
60
Registered
2025-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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: intravenous Dexmedetomidine 1mcg/kg: intravenous infusion of dexmedetomidine 1mcg/kg in 100 ml NS over 15 to 20 minutes 5 minutes before induction of general anaesthesia Control Interve

Sponsors

Smt Bhikiben Kanjibhai Shah Medical Institute and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to give written and informed consent male and females of age group 18 to 55 years of age patients belonging to ASA physical status 1 and 2 patients posted for elective surgeries under general anaesthesia

Exclusion criteria

Exclusion criteria: patients unwilling to participate in the study patients with crdiovascular, cerebrovascular, hepatic and renel diseases patients having arrhytmias or heart block psychiatric patients pregnancy and lactating patients patients taking beta blockers history of allergy to the study drugs BM! more than 30 patients with ASA physical status of 3 and above patients with suspected difficult airway and Mallampatti grade 3 and 4

Design outcomes

Secondary

MeasureTime frame
to study sedation status using RAMSAY sedation scoreTimepoint: post operatively for every 30 minutes till RAMSAY sedation score of 2 is achieved

Primary

MeasureTime frame
to study hemodynamic response during laryngoscopy and endotracheal intuabtionTimepoint: baseline after administration of the test drug after induction at laryngoscopy and intubation at 1 min after intubation at 3 mins after intubation at 5 mins after intubation

Countries

India

Contacts

Public ContactDr Sara Mary Thomas

Smt. Bhikiben Kanjibhai Shah Medical Institute and Research Centre

sara.cinosh@gmail.com9646500158

Outcome results

None listed

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