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Database of Interstitial Lung Diseases

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified December 2005 by St. Antonius Hospital.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00267800
First Posted: December 21, 2005
Last Update Posted: August 8, 2008
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.
Information provided by:
St. Antonius Hospital
  Purpose
The cause of most interstitial lung diseases (ILDs) is still unknown. Further research, for example 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 cause of ILDs.

Condition
Interstitial Lung Diseases

Study Type: Observational
Official Title: Registration of Clinical Data and DNA/Serum of Patients With Interstitial Lung Diseases (ILD)

Resource links provided by NLM:


Further study details as provided by St. Antonius Hospital:

Estimated Enrollment: 100000
Study Start Date: January 2006
Detailed Description:

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.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of an ILD, as stated by the American Thoracic Society (ATS)
  Contacts and Locations
Information from the National Library of Medicine

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


Locations
Netherlands
St. Antonius Hospital
Nieuwegein, Netherlands, 3435CM
Diakonessenhuis
Utrecht, Netherlands, 3508 TG
Mesos Medisch Centrum
Utrecht, Netherlands, 3527 CE
UMC Utrecht
Utrecht, Netherlands, 3584 CX
Sponsors and Collaborators
St. Antonius Hospital
Investigators
Principal Investigator: J.M.M. van den Bosch, M.D. St. Antonius Hospital
Principal Investigator: J.C. Grutters, M.D. St. Antonius Hospital
  More Information

Additional Information:
ClinicalTrials.gov Identifier: NCT00267800     History of Changes
Other Study ID Numbers: R05.08/A
First Submitted: December 19, 2005
First Posted: December 21, 2005
Last Update Posted: August 8, 2008
Last Verified: December 2005

Keywords provided by St. Antonius Hospital:
Lung disease, Interstitial
Sarcoidosis
Pulmonary fibrosis

Additional relevant MeSH terms:
Lung Diseases
Lung Diseases, Interstitial
Respiratory Tract Diseases