Experience with Bedside Surgical procedure of creating an opening in the Windpipe at an Adult Intensive care unit in Tertiary Hospital of Northern India

Active, not recruiting

• Conditions: All patients who underwent percutaneous tracheostomy in Intensive care unit

• Registration Number: CTRI/2012/12/003224
• Lead Sponsor: MedantaThe Medicity

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" /

Detailed Description

Not available

Study Timeline

• Study Start: 2012-12-20
• Last Update Posted: 2021-06-16

Recruitment & Eligibility

• Status: Closed to Recruitment of Participants
• Sex: All
• Target Recruitment: 800

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.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intraoperative, immediate (upto 8 hrs.) & short term (8-24 hrs) major & minor complications	34 months

Secondary Outcome Measures

Name	Time	Method
Duration of ICU stay and mortality	34 months

Trial Locations

Locations (1)

Medanta Institute of Critical care and Anesthesia; 🇮🇳 Gurgaon, HARYANA, India

Medanta Institute of Critical care and Anesthesia

🇮🇳Gurgaon, HARYANA, India

DrYatin Mehta

Principal investigator

9971698149

yatin.mehta@medanta.org