Database of Interstitial Lung Diseases
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00267800|
Recruitment Status : Unknown
Verified December 2005 by St. Antonius Hospital.
Recruitment status was: Active, not recruiting
First Posted : December 21, 2005
Last Update Posted : August 8, 2008
|Condition or disease|
|Interstitial Lung Diseases|
Protocol title: 'Registration of clinical data and DNA of patients with Interstitial Lung Disease (ILD)' Rationale: The etiopathogenesis of most Interstitial Lung Diseases (ILDs) is still unknown. Further research, e.g. to determine predisposing genetic factors, is therefore needed. A database with relevant clinical data and DNA/serum samples of ILD patients could facilitate future research on the etiopathogenesis of ILDs.
Objective: Availability of relevant clinical data and DNA/serum samples of ILD patients in a database. Those data can be used for future research.
Study design: A prospective observational study
Study population: Patients diagnosed with ILD attending the pulmonology department in participating hospitals.
Intervention: a blood sample is taken from each patient. Furthermore, additional information is collected from the medical file.
Main study parameters/endpoints: DNA and serum sample, demographic variables, medical information, occupational history and hobbies.
Nature and extent of the burden and risks associated with participation, group relatedness: two tubes of blood will be drawn from the patients. The risks of drawing blood from a vein are minimal.
|Study Type :||Observational|
|Enrollment :||100000 participants|
|Official Title:||Registration of Clinical Data and DNA/Serum of Patients With Interstitial Lung Diseases (ILD)|
|Study Start Date :||January 2006|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00267800
|St. Antonius Hospital|
|Nieuwegein, Netherlands, 3435CM|
|Utrecht, Netherlands, 3508 TG|
|Mesos Medisch Centrum|
|Utrecht, Netherlands, 3527 CE|
|Utrecht, Netherlands, 3584 CX|
|Principal Investigator:||J.M.M. van den Bosch, M.D.||St. Antonius Hospital|
|Principal Investigator:||J.C. Grutters, M.D.||St. Antonius Hospital|