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Clinical Trials/CTRI/2020/12/030029
CTRI/2020/12/030029Not yet recruitingNot Applicable

Comparison of oxygenation using venturi mask and high flow nasal cannula in patients undergoing minor surgery under total intravenous anaesthesia.

DMCH1 site in 1 country100 target enrollmentStarted: December 30, 2020Last updated:
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Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
DMCH
Enrollment
100
Locations
1
Primary Endpoint
Incidence of Hypoxia(saturation falling less than 90%).
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Comparison of oxygenation using venturi mask and high flow nasal cannula in patients undergoing minor surgery under total intravenous anaesthesia.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Not Applicable

Eligibility Criteria

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

Inclusion Criteria

  • •ASA 1 and 2 patients patients withBMI<40kg/m2.

Exclusion Criteria

  • •Morbid obese patients.
  • •patients having pre procedure saturation <90% peripheral vascular diseases.
  • •Psychiatric/neurological diseases.
  • •Allergic to drugs used in general anaesthesia.
  • •Severe renal,cardiac,respiratory diseases.

Outcomes

Primary Outcomes

Incidence of Hypoxia(saturation falling less than 90%).

Time Frame: Incidence of hypoxia is assesed at every 2 minutes during intraoperative period and at every 10 minutes during postoperative period upto 1 hour.

Secondary Outcomes

  • Haemodynamic instability(more than 20percent fluctuation from baseline)(Need for airway manoeuvres or adjuncts.)

Investigators

Sponsor
DMCH
Sponsor Class
Private medical college

Study Sites (1)

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