- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01154998
Case-Control Study of Fibrotic Interstitial Lung Disease (ILD) and Cardiac Disease / Interventions.
June 30, 2010 updated by: St George's Healthcare NHS Trust
Case-Control Study of Fibrotic Interstitial Lung Disease and it's Association With Cardiac Disease or Cardiac Intervention.
There is a rare condition causing scarring of the lungs termed interstitial lung disease.
This comprises a group of conditions which can be divided into separate diseases.
The aim of this study is compare a group of patients (the cases) with 2 types of this disease (fibrotic non-specific interstitial pneumonia (NSIP) and idiopathic pulmonary fibrosis (IPF)) with patients without the disease.
The study will look at the 2 groups and their exposures to factors such as medications, smoking, previous jobs, previous medical problems and specifically heart disease and any operations or procedures involving the heart.
There have been previous studies showing a link between heart disease and scarring of the lungs.
This study will look at whether this association is stronger in one or the other type of lung scarring diseases.
Study Overview
Status
Unknown
Study Type
Observational
Enrollment (Anticipated)
360
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
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London, United Kingdom, SW17 0QT
- St George's Hospital
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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 and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Cases - patients with IPF or UIP.
Controls - hospital clinic attenders.
Description
Inclusion Criteria:
- idiopathic fibrotic lung disease
Exclusion Criteria:
- non idiopathic fibrotic lung disease
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
Cohorts and Interventions
Group / Cohort |
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Controls
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Cases
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
July 1, 2010
Primary Completion (ANTICIPATED)
January 1, 2011
Study Completion (ANTICIPATED)
April 1, 2011
Study Registration Dates
First Submitted
June 30, 2010
First Submitted That Met QC Criteria
June 30, 2010
First Posted (ESTIMATE)
July 1, 2010
Study Record Updates
Last Update Posted (ESTIMATE)
July 1, 2010
Last Update Submitted That Met QC Criteria
June 30, 2010
Last Verified
June 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10/H1102/46
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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