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Clinical Trials/CTRI/2024/01/061870
CTRI/2024/01/061870Not yet recruitingNot Applicable

Major Adverse Peri-Intubation events during intubation of critically ill patients - A prospective observational study in south Asian population

Nizams Institute of Medical Sciences1 site in 1 country200 target enrollmentStarted: February 14, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
200
Locations
1
Primary Endpoint
To determine the incidence of major adverse peri-intubation events defined as severe hypoxemia SpO2 less than 80%, Cardiac arrest, Cardiovascular instability, new requirement for or increase in vasopressors

Study Overview

Brief Summary

This study is designed to assess the incidence and types of major adverse peri-intubation events in critically ill patients with appropriate inclusion and exclusion criteria. All the patients intubated under anesthesia residents will be included and data taken from medical records for a period of one year. Parameters studied will be reason for intubation,intubator details, complications present during assessment, hemodynamics in peri-intubation period, respiratory status, method of preoxygenation, drugs used for intubation, equipment, success rate of intubation, complications. Statistical analysis will be performed using SPSS version 24

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Critically ill patients with life threatening impairment requiring endotracheal intubation
  • •In-hospital emergency intubations occurring in EMD, ICU, wards.

Exclusion Criteria

  • •Patients who underwent out of hospital intubation
  • •Intubations following cardiac arrest
  • •Patients with saturations less than 80% at the end of preoxygenation.

Outcomes

Primary Outcomes

To determine the incidence of major adverse peri-intubation events defined as severe hypoxemia SpO2 less than 80%, Cardiac arrest, Cardiovascular instability, new requirement for or increase in vasopressors

Time Frame: Baseline, At the time of intubation and 10 minutes later

Secondary Outcomes

  • 1. Incidence of cardiac arrhythmias(2. Incidence of difficult intubation)

Investigators

Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr J Kavitha

Nizams Institute of Medical Sciences

Study Sites (1)

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