Skip to content

Mortality in Non-cystic Fibrosis Bronchiectasis

Mortality in Non-cystic Fibrosis Bronchiectasis: a Long-term Cohort Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01792427
Enrollment
253
Registered
2013-02-15
Start date
2006-06-30
Completion date
2012-12-31
Last updated
2013-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-cystic Fibrosis Bronchiectasis

Brief summary

In this study we analyzed the overall survival for all newly diagnosed patients with non-cystic fibrosis bronchiectasis from June 2006 onwards. The investigators wanted to confirm the known risk factors such as age, gender, smoking history and Pseudomonas aeruginosa and evaluate the impact on survival of etiology, number of different bacteriological species in retrospective and prospective sputa, azithromycin use and presence/development of pulmonary hypertension.

Interventions

None listed

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with clinically significant and radiologically proven bronchiectasis * Chest CT scan confirming the presence of bronchiectatic lesions and had symptoms of chronic productive cough * Bronchiectasis was deemed to be present if there was one or more of the following criteria: a bronchoarterial ratio greater than 1, lack of tapering of the bronchi and visualization of bronchi within 1 cm of costal or paravertebral pleura or abutting the mediastinal pleura

Exclusion criteria

* diagnosis of cystic fibrosis * underlying tumoral problem causing the bronchiectatic lesions (postradiotherapy, secondary immunodeficiency due to chemotherapy or postinfectious due to tumoral obstruction) * patients with asymptomatic traction bronchiectasis caused by interstitial lung disease

Design outcomes

Primary

MeasureTime frame
overall survival6 years 4 months

Secondary

MeasureTime frameDescription
risk factor identification for NCFB6 years 4 monthsThe investigators wanted to confirm the known risk factors such as age, gender, smoking history and Pseudomonas aeruginosa.

Other

MeasureTime frameDescription
Identify cause of death6 years 4 monthsIf death occurred, the patient file was reassessed to identify cause of death.
risk factor identification for the survival of NCFB6 years 4 monthsThe investigators will evaluate the impact of etiology, number of different bacteriological species in retrospective and prospective sputa, azithromycin use and presence/development of pulmonary hypertension on survival .

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026