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Evaluation of different equipments to find out the best equipment for awake tracheal intubation.

Phase 1
Conditions
Health Condition 1: O- Medical and SurgicalHealth Condition 2: Z533- Procedure converted to open procedure
Registration Number
CTRI/2024/05/067657
Lead Sponsor
Government Institute of medical science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Inclusion criteria-

1 ASA grade I / II.

2 Age between 18-65 years.

3 Patient undergoing surgeries requiring general anaesthesia with intermittent positive pressure ventilation in adult paralyzed patients.

4.Patients with anticipated difficult airway.

Exclusion Criteria

? History of

upper gastro-intestinal surgery.

bleeding or clotting abnormalities.

oesophageal trauma ,

oesophageal varices or evidence of upper gastro-intestinal bleed

hiatus hernia, gastroesophageal reflux disease.

?Pregnancy.

?Patient having significant medical diseases in term of cardiac, respiratory, hepatic,

?renal, etc.;

cervical spine pathology

?upper airway pathology;

?Difficult front of neck access.

? who had refused to give consent.

?Risk of regurgitation, and airway surgeries will be excluded

from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the time required for awake intubation using fiberoptic bronchoscope, C-MAC Videolaryngoscope and kingvision videolaryngoscope.Timepoint: 0MINUTE,5 MINUTE,10MINUTE
Secondary Outcome Measures
NameTimeMethod
First attempt success rate-Number of patients which could be intubated in a single attempt with each of the study device will be recordedTimepoint: 0MINUTE,5MINUTE,10MINUTE
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