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Clinical Trials/CTRI/2020/07/026314
CTRI/2020/07/026314Not yet recruitingNot Applicable

Comparison of Pre-oxygenation with High Flow Nasal Cannula and Facemask in patients undergoing Rapid sequence induction of Anaesthesia for Elective surgery.

ABVIMS and Dr RML Hospital1 site in 1 country100 target enrollmentStarted: February 7, 2020Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Oxygen saturation at Baseline and its changes during intubation procedures.
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

In this study ,we compare pre-oxygenation with high flow nasal cannula and facemask in patients undergoing rapid sequence induction of general anaesthesia in elective surgery.

and we also compare end tidal oxygen concentration as measure of effective pre-oxygentaion with high flow nasal cannula and facemask in patients undergoing rapid sequence induction of general anaesthesia in elective surgery.

Study Design

Study Type
Interventional
Allocation
Stratified block randomization

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •ASA Physical Status I,II.

Exclusion Criteria

  • •Upper airway pathology.
  • •Cervical Spine fracture.
  • •Facial fracture and Maxillofacial abnormality.
  • •Inter incisor distance <3cm.
  • •Patient with Past history of Difficult intubation.

Outcomes

Primary Outcomes

Oxygen saturation at Baseline and its changes during intubation procedures.

Time Frame: oxygen saturation at Baseline and its changes at 3 end points. | T1- After pre-oxygenation(4 minutes). | T2- At the time of laryngoscopy(5 minutes). | T3-One minute after intubation(6 minutes).

Secondary Outcomes

  • End Tidal oxygen concentration.(Apnoea time measurement.)

Investigators

Sponsor
ABVIMS and Dr RML Hospital
Sponsor Class
Research institution and hospital

Study Sites (1)

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