riSk Factors fOR neCk phlEgmon afteR pErcutaneous tRacheostomy in ICU
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
| Condition(s) | Tracheostomy Complication, Quality of Life |
|---|---|
| Status | Recruiting |
| 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 |
| Who can participate | 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 |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Azienda Usl di Bologna |
| Locations | Bologna, Italy |
| Start date | 2018-08-09 |
| NCT ID | NCT06552676 |
| Official listing | https://clinicaltrials.gov/study/NCT06552676 |