- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01906047
Impact of Chronic Air Pollution on Non-cystic Fibrosis Bronchiectasis
July 18, 2013 updated by: Dr. Lieven Dupont, Universitaire Ziekenhuizen KU Leuven
We aim at investigation the impact of chronic air pollution exposure on non-cystic fibrosis bronchiectasis outcome.
Study Overview
Status
Completed
Conditions
Detailed Description
- Patient files will be search for time of death and cause of death.
- Other variables will be collected: bacterial culture results, therapy, gender, age, etc.
- These data will be linked with pollution data: trafic load, distance to major road, etc.
Study Type
Observational
Enrollment (Actual)
189
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Vlaams-Brabant
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Leuven, Vlaams-Brabant, Belgium, 3000
- UZ Leuven
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with a HRCT diagnosis of bronchiectasis and do not have a diagnosis of cystic fibrosis.
They also need to have typical bronchiectatic disease (recurrent infections and sputum).
Description
Inclusion Criteria:
- HRCT diagnosis of bronchiectasis
- recurrent infections or chronic sputum production
- patients between 18 and 65 years old.
Exclusion Criteria:
- Cystic Fibrosis
- Tumoral disease
- Traction bronchiectasis due to interstitial lung disease
- patients older than 65 years or younger than 18 years at recruitment
- COPD
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Death
Time Frame: 6 years
|
From June 2006 till October 2012, enrolled patients' medical file will be screened if death has occurred.
If so, cause of death will be search for in the patients' file.
|
6 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Lieven J Dupont, MD, PhD, UZ Leuven
- Principal Investigator: Pieter C Goeminne, MD, UZ Leuven
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2006
Primary Completion (Actual)
October 1, 2012
Study Completion (Actual)
April 1, 2013
Study Registration Dates
First Submitted
July 18, 2013
First Submitted That Met QC Criteria
July 18, 2013
First Posted (Estimate)
July 23, 2013
Study Record Updates
Last Update Posted (Estimate)
July 23, 2013
Last Update Submitted That Met QC Criteria
July 18, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NCFB chronic pollution
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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