Segmental Bronchoalveolar Lavage
Asthma, Pulmonary Fibrosis
About this trial
This is an observational trial for Asthma focused on measuring Cystic Fibrosis, Healthy Volunteers, Asthma, Normal Volunteer, Chronic Lung Disease
Eligibility Criteria
INCLUSION CRITERIA: Patients and research volunteers will be accepted for bronchoscopy and bronchoalveolar lavage only if their heath status will not be compromised by the procedure. Examples of disease that may be studied under this protocol include alpha-1 antitrypsin deficiency; lymphangioleiomyomatosis and the cystic lung disease; pulmonary fibrosis; and sarcoidosis. EXCLUSION CRITERIA: Patients or research volunteers with abnormalities that contraindicate, or increase the risk of, fiberoptic bronchoscopy and bronchoalveolar lavage, including a history of allergy to atropine, lidocaine, or other topical anesthetics or premedications; FEV(1) less than 0.8 liters; PaO(2), on supplemental 02, of less than 70 mmHg or PaCO(2) greater than 45 mmHg; presence of uncorrected clotting disorder, uncontrolled hypertension, significant cardiac disease, renal or liver failure; metastatic disease; hematologic disorders such as severe anemia (hemoglobin less than or equal to 7 g/ml), granulocytopenia, or platelet disorders. Patients or research volunteers with a positive serum test for human immunodeficiency virus or hepatitis B or C. The rationale for excluding participation on the basis of HIV seropositivity is because of the known effects of HIV on the lungs. Patients or research volunteers who are pregnant or lactating. Patients or research volunteers incapable of giving informed consent.
Sites / Locations
- National Institutes of Health Clinical Center, 9000 Rockville Pike