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Clinical Trials/CTRI/2012/12/003224
CTRI/2012/12/003224Active, not recruitingNot Applicable

Experience with Percutaneous Tracheostomy at an adult intensive care institute in northern India: A descriptive study

MedantaThe Medicity1 site in 1 country800 target enrollmentStarted: December 20, 2012Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
800
Locations
1
Primary Endpoint
Intraoperative, immediate (upto 8 hrs.) & short term (8-24 hrs) major & minor complications
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

This study will enable us to assess the incidence of early complications of percutaneous tracheostomy and provide data which can be used for future studies, The study will also explore optimum  timing & technique of percutaneous dilational tracheostomy  for specific patientsxml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 99.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •All patient above 18years of age and those who underwent percutaneous tracheostomy in Intensive care units between November,2009 and June 2012 are enrolled.

Exclusion Criteria

  • •Patient leaving against medical advise soon after percutaneous tracheostomy Patient shifted to outside ICU soon after percutaneous tracheostomy.

Outcomes

Primary Outcomes

Intraoperative, immediate (upto 8 hrs.) & short term (8-24 hrs) major & minor complications

Time Frame: 34 months

Secondary Outcomes

  • Duration of ICU stay and mortality(34 months)

Investigators

Sponsor
MedantaThe Medicity
Sponsor Class
Private hospital/clinic

Study Sites (1)

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