riSk Factors fOR neCk phlEgmon afteR pErcutaneous tRacheostomy in ICU (SORCERER)

Azienda Usl di Bologna

Status: Enrolling

Conditions: Quality of Life; Tracheostomy Complication

Treatments: Procedure: Percutaneous tracheostomy

Study type: Observational

Funder types: Other

Identifiers

NCT06552676

SORCERER - 24088

Details and patient eligibility

About

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

Enrollment: 300 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age greater than 18 years
• Presence of indication for tracheostomy

Exclusion criteria

• Failure of the percutaneous tracheostomy technique or recourse to surgical tracheostomy

Trial design

300 participants in 1 patient group

Percutaneous tracheostomy

Description:

Patients receiving percutaneous tracheostomy for any reason during their ICU stay

Treatment:

Procedure: Percutaneous tracheostomy