C34
Conditions
Interventions
Group 1: Data of all patients undergoing electromagneticbronchoscopy will be collected retrospectively in a database.
The following data will be collected by the principal investigator and co-investig
Sponsors
UNIVERSITÄTSKLINIKUM FREIBURG Department Chirurgie Klinik für Thoraxchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - peripheral pulmonary lesion - Patients undergoing ENB 2016-2019 - signed informed consent of the patient
Exclusion criteria
Exclusion criteria: no written consent, bronchoscopy without ENB
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint is the procedure time | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are diagnostic yield, Complications (e.g. Pneumothorax, intrapulmonal haemorrhage, Pneumonia), Nodule configuration and lung function parameters. | — |
Countries
Germany
Contacts
Public ContactCaroline Hess
Universitätsklinikum FreiburgKlinik für Thoraxchirurgie
Outcome results
None listed