Study 2 of 8 for search of: Qatar
Previous Study Return to Search Results Next Study

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Lung Disease Collection (Qatar): Evaluation of the Lungs of Individuals With Lung Disease (Q-LD)
This study is currently recruiting participants.
Verified by Weill Medical College of Cornell University, September 2008
Sponsors and Collaborators: Weill Medical College of Cornell University
Weill Cornell Medical College in Qatar
Hamad Medical Corporation
Information provided by: Weill Medical College of Cornell University
ClinicalTrials.gov Identifier: NCT00504738
  Purpose

The purpose of this protocol is to obtain biologic samples from the blood and lungs from patients with lung diseases in order to study the causes and indications of these disorders, learn how these lung disease manifest and progress, and how the lung disease can be treated.


Condition
Lung Disease
Chronic Obstructive Pulmonary Disease (COPD)
Asthma

MedlinePlus related topics: Asthma COPD (Chronic Obstructive Pulmonary Disease)
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Evaluation of the Lungs of Individuals With Lung Disease With Segmental Bronchopulmonary Lung Lavage, Bronchial Brushing, and Bronchial Wall Biopsy (Qatar)

Further study details as provided by Weill Medical College of Cornell University:

Biospecimen Retention:   Samples With DNA

Biospecimen Description:

Estimated Enrollment: 200
Study Start Date: April 2006
Detailed Description:

The lung diseases are disorders associated with functional and/or structural derangements to the alveolar structures, airways, pulmonary blood vessels, pleura and/or mediastinum. The purpose of this protocol is to obtain biologic materials from the blood and lungs from these patients in order to: (1) develop an understanding of the etiology and pathogenesis of these disorders; and (2) identify individuals who will be suitable candidates for other protocols such as those involving investigational new drugs. As such, this protocol is part of the "infrastructure" for all of our human lung-related studies such as genomic/gene expression studies of airway epithelium and alveolar macrophages in all individuals with chronic obstructive lung disease (COPD), asthma, bronchogenic carcinoma, and pulmonary fibrosis compared to normal non-smokers and smokers, and studies of mediators in bronchoalveolar lavage fluid.

This protocol, to be carried out at Weill Cornell Medical College - Qatar and Hamad Medical Corporation, Qatar, parallels a similar approved protocol IRB #0005004440, entitled, "Evaluation of the Lungs of Individuals with Lung Disease with Segmental Bronchopulmonary Lung Lavage, Bronchial Brushing, and Bronchial Wall Biopsy", ongoing at Weill Cornell Medical College - New York.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Recruitment will be from the patients of the Hamad Medical Corporation and others as relevant. The source of potential subjects will be the population of potential subjects with lung disease, as defined by the elegibility criteria, in Qatar. Accrual will be random with no bias as to gender or racial/ethnic group.

Criteria

Inclusion Criteria:

Inclusion/Exclusion criteria for Part A

  • Must provide informed consent
  • Males and females, age 18 years and older
  • Evidence of lung disease by at least one of the following:

    1. symptoms consistent with pulmonary disease;
    2. chest X-rays and/or chest CT consistent with lung disease;
    3. pulmonary function tests consistent with lung disease;
    4. lung biopsy consistent with lung disease;
    5. family history of lung disease;
    6. diseases of organs with known association with lung disease; and
    7. individuals suspected of having lung disease based on history and/or physical examination
  • Undergoing fiberoptic bronchoscopy as dictated by their standard clinical care

Exclusion Criteria:

  • Patient refuses consent.

Patients enrolled in Part A of the protocol will not undergo screening procedures/tests. These patients are undergoing a fiberoptic bronchoscopy as dictated by their standard clinical care and additional samples will be taken for research purposes.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00504738

Contacts
Contact: Charleen Hollmann, PhD, RN 646-962-2672 chollman@med.cornell.edu
Contact: Mary Yeotsas, BA 646-962-2672 mey2003@med.cornell.edu

Locations
Qatar
Hamad Medical Corporation Recruiting
Doha, Qatar
Contact: Amani Ma'ayah, MS, Pharm     + 974-492-8405     asm2004@qatar-med.cornell.edu    
Contact: Abeer Gohar, BA     + 974-492-8407     abg2004@qatar-med.cornell.edu    
Principal Investigator: Hisham A Sattar, MD            
Principal Investigator: Lotfi Chouchane, PhD            
Sponsors and Collaborators
Weill Medical College of Cornell University
Weill Cornell Medical College in Qatar
Hamad Medical Corporation
Investigators
Principal Investigator: Ronald G. Crystal, MD Weill Cornell Medical College, New York and Qatar
  More Information

Responsible Party: Weill Cornell Medical College, Department of Genetic Medicine ( Dr. Ronald G. Crystal )
Study ID Numbers: 0604008489, HMC RC392/2006
Study First Received: July 19, 2007
Last Updated: September 15, 2008
ClinicalTrials.gov Identifier: NCT00504738  
Health Authority: United States: Institutional Review Board;   Qatar: Hamad Medical Corporation Research Committee

Keywords provided by Weill Medical College of Cornell University:
lung disease
chronic obstructive pulmonary disease (COPD)
asthma
smokers
non-smokers

Study placed in the following topic categories:
Hypersensitivity
Lung Diseases, Obstructive
Respiratory Tract Diseases
Lung Diseases
Hypersensitivity, Immediate
Asthma
Respiratory Hypersensitivity
Pulmonary Disease, Chronic Obstructive

Additional relevant MeSH terms:
Immune System Diseases
Bronchial Diseases

ClinicalTrials.gov processed this record on January 16, 2009