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Trials / Completed

CompletedNCT07385040

Comparison of IV Lignocain and IV Dexmedetomidine for Attenuation of Laryngoscopic Stress Response to Direct Laryngoscopy

Comparison of Intravenous Lignocain and Intravenous Dexmedetomidine for Attenuation of Hemodynamic Stress Response to Direct Laryngoscopy and Endotracheal Intubation

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
62 (actual)
Sponsor
Shaheed Mohtarma Benazir Bhutto Institue of Trauma · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Hemodymanic stress response to direct laryngoscopy and endotracheal intubation is a known phenomenon that occur in almost every patient undergoing general anesthesia before surgical procedure. This response leads to sudden rise in heart rate and blood pressure which may cause serious complications in compromised patients having cardiovascular diseases. There are certain drugs which are used to blunt this response and to prevent the life threatening complications. Intravenous Lignocain is commonly used drug to blunt the laryngoscopic response in our setup. Intravenous Dexmedetomidine is a newer and rarely used drug to prevent stress response to direct laryngoscopy and endotracheal intubation. This study aims to compare the efficacy of both the drugs to provide better control of complications like Arrythmias, stroke and cardiovascular instability.

Conditions

Interventions

TypeNameDescription
DRUGIntravenous Dexmedetomidine infusionDexmedetomidine infusion with dose of 10mics/kg given 10min before induction
DRUGIntravenous LignocainIntravenous ligoncain 1.5mg/kg given 90sec before induction.

Timeline

Start date
2023-04-13
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2026-02-03
Last updated
2026-02-03

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT07385040. Inclusion in this directory is not an endorsement.

Comparison of IV Lignocain and IV Dexmedetomidine for Attenuation of Laryngoscopic Stress Response to Direct Laryngoscop (NCT07385040) · Clinical Trials Directory