Risk Factors for Neck Phlegmon After Percutaneous Tracheostomy in ICU

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

Primary Purpose: To investigate the incidence and risk factors related to the appearance of tracheal phlegmon in patients undergoing percutaneous tracheostomy. Participant Population/Primary Condition: Patients admitted to Intensive Care Main Questions Aims to Answer: 1. \- What are the risk factors associated with the development of tracheal phlegmon percutaneous tracheostomy? 2. \- How does the appearance of tracheal phlegmon impact intensive care stay, hospital stay, mortality, and Health-related quality of life? Participants will be followed up after undergoing tracheostomy for 7 days to identify eventual phlegmons. At the two-year follow-up, the health-related quality of life will be assessed

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age greater than 18 years

• Presence of indication for tracheostomy

Locations
Other Locations
Italy
Maggiore Hospital Carlo Alberto Pizzardi
RECRUITING
Bologna
Contact Information
Primary
Lorenzo Gamberini, MD
gamberini6@ausl.bologna.it
+393403550540
Time Frame
Start Date: 2018-08-09
Estimated Completion Date: 2025-01-31
Participants
Target number of participants: 300
Treatments
Percutaneous tracheostomy
Patients receiving percutaneous tracheostomy for any reason during their ICU stay
Related Therapeutic Areas
Sponsors
Leads: Azienda Usl di Bologna

This content was sourced from clinicaltrials.gov