Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06552676

riSk Factors fOR neCk phlEgmon afteR pErcutaneous tRacheostomy in ICU

Risk Factors for Neck Phlegmon After Percutaneous Tracheostomy in ICU

Status
Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
Azienda Usl di Bologna · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
PROCEDUREPercutaneous tracheostomyPercutaneous tracheostomy is a widely used technique in intensive care. It involves creating a passage between the tracheal lumen and the outside, through which a cannula is placed.

Timeline

Start date
2018-08-09
Primary completion
2024-12-31
Completion
2025-01-31
First posted
2024-08-14
Last updated
2024-08-14

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06552676. Inclusion in this directory is not an endorsement.