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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06213116
Other study ID # USM/JEPeM/21080580
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2021
Est. completion date July 1, 2023

Study information

Verified date May 2024
Source Universiti Sains Malaysia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparing the efficacy between Lignocaine given via MADgic Atomizer and Lignocaine Pump Spray pre endotracheal intubation in adult undergoing General Anesthesia.


Description:

Comparing the efficacy of Lignocaine given via 2 device (Lignocaine Spray and MADGIC Atomizer) on hemodinamic parameters postintubations and severity grading of post operative sore throat, cough and hoarseness of voice.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date July 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Adult with the age of 18 to 65 years old - Gender of both male and female - Planned for elective surgery scheduled at General Operation Theatre that require elective intubation for general anesthesia - American Society Anaesthesiologist (ASA) preoperative physical status assessment of 1 and 2 - Airway assessment Malampati scoring 1and 2. Exclusion Criteria: - Pregnancy - Known allergy or hypersensitivity to Lignocaine - Pre existing sore throat or hoarseness of voice identified during preoperative assessment. - The use of airway device other than endotracheal tube (ETT) such Laryngeal Mask airway/Supraglottic Device' - Oral and neck surgery

Study Design


Intervention

Device:
MADgic Atomizer
Device to deliver directly lignocaine
Lignocaine pump spray
Lignocaine 30 mg (3 puffs) given via 10mg Lignocaine Pump Spray prior to endotracheal intubation

Locations

Country Name City State
Malaysia University of Science Malaysia Hospital Kubang kerian Kelantan

Sponsors (1)

Lead Sponsor Collaborator
Universiti Sains Malaysia

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Severity Grading of Post Operative Sore Throat Numbers of participants complaining incidence of sore throat postoperatively 24 hours
Secondary Severity Grading of Post Operative Cough Numbers of participants complaining incidence of cough postoperatively 24 hours
Secondary Severity grading of Hoarseness of voice Numbers of participants complaining incidence of hoarseness of voice postoperatively 24 hours
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