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Trial Title: Comparison Between McGrath and Macintosh Laryngoscopes for DLT Intubation in Thoracic Surgery Patients.

NCT ID: NCT05988736

Condition: Thoracic Diseases
Thoracic Neoplasms
Thoracic Empyema

Conditions: Official terms:
Empyema
Empyema, Pleural
Thoracic Neoplasms
Thoracic Diseases
Aortic Dissection

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Other

Masking: Single (Participant)

Intervention:

Intervention type: Device
Intervention name: MaCintosh Laryngoscope (DL)
Description: A conventional Laryngoscope. It is battery powered, with a detachable MaCintosh blade that contains a light source.
Arm group label: Group A

Intervention type: Device
Intervention name: McGrath Laryngoscope (VL)
Description: A video Laryngoscope that has a high-resolution video camera, and a light source at the cone end of the blade allowing for direct and indirect viewing of the glottis
Arm group label: Group B

Summary: The goal of this RCT is to compare outcome with McGrath vs Macintosh laryngoscopes among patients undergoing thoracic surgery. The main questions it aims to answer are, 1. Rate of successful intubation at first attempt and 2. Time for intubation required with each device. Participants are required to sign the informed consent for, they will be placed in two groups, Group A: Macintosh (DL) Group B: McGrath (VL) Researchers will compare in Group A: Macintosh (DL) and Group B: McGrath (VL) the differences in rate of successful intubation at first attempt and time for intubation required with each device.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Age 18-65 years - American Society of Anaesthesiologists physical status (ASA) I, II, III - Elective thoracic surgery patients, requiring one lung ventilation. Exclusion Criteria: - Patients requiring rapid sequence induction - Patients with a structural problem in the airway on chest radiography - History of difficult intubation - Planned tracheostomy \ the presence of a tracheostomy - Patients with a BMI >35 kg\m2. Who at risk of regurgitation\ Aspiration - Anticipated Difficult Airway (Mallampati IV) - Pre-existing sore throat or hoarseness, or recent respiratory infection (<15 days)

Gender: All

Minimum age: 18 Years

Maximum age: 65 Years

Healthy volunteers: No

Locations:

Facility:
Name: Aga Khan University Hospital

Address:
City: Karachi
Country: Pakistan

Status: Recruiting

Contact:
Last name: sadique Wadho, MBBS

Phone: +923322792932
Email: sadique.ali@aku.edu

Contact backup:
Last name: Khalid Samad, MBBS. FCPS

Phone: +923343311603
Email: khalid.samad@aku.edu

Investigator:
Last name: sadique Wadho, MBBS
Email: Principal Investigator

Investigator:
Last name: Khalid Samad, MBBS, FCPS
Email: Principal Investigator

Start date: June 15, 2022

Completion date: December 31, 2023

Lead sponsor:
Agency: Aga Khan University
Agency class: Other

Source: Aga Khan University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05988736

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