Interstitial Lung Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People diagnosed with alpha-1 antitrypsin (AAT) deficiency who have a confirmed high-risk genetic type, along with symptoms, chest x-ray results, and breathing test results that show lung disease — this includes both current smokers (at least 1 pack per day for 2 or more years) and non-smokers or ex-smokers who have not smoked for 3 or more years.
- People with chronic obstructive pulmonary disease (a long-term lung condition) who have symptoms, chest x-ray results, and breathing test results consistent with lung disease — including both current smokers and people who have never smoked or stopped smoking 3 or more years ago.
- People with cystic fibrosis who have a known gene change linked to the condition, or whose symptoms and clinical features are consistent with cystic fibrosis; children with cystic fibrosis aged 8 and over may also be included.
- People already diagnosed with sarcoidosis, mycobacterial infections, tuberous sclerosis complex (TSC), cystic lung diseases, lymphangioleiomyomatosis, lymphatic disorders, a history of pneumothorax, pulmonary fibrosis, asthma, histiocytosis X, or diabetes mellitus.
- Relatives of patients with the conditions covered by this trial may also be seen under this study.
- Children aged 2 and over with lymphangiomatosis may be included.
- People with asthma may be enrolled at Suburban Hospital specifically.
- Healthy volunteers with no lung disease (for example, people with rheumatoid arthritis but no lung involvement) may join as a pulmonary control group.
- Healthy volunteers with no history of diabetes, coronary artery disease, or lung disease may join as a diabetes control group.
- Pregnant or nursing women may be included in the study, though certain procedures will not be carried out during pregnancy or while nursing, including breathing tests, the six-minute walk test, bronchoscopy, thoracentesis, and imaging tests involving contrast dye or radiation such as chest x-rays, CT scans, and MRIs.
- People with abnormalities in certain cell-level chemical processes known as ADP-ribosylation may be included; children aged 2 and over may be included if they have a known defect in this process, or if a family member has such a defect and the child may be affected.
Who may not be able to join:
- People younger than 18 or older than 90, with specific exceptions: NIH patients with the conditions described in this trial may be eligible from age 16; children with cystic fibrosis may be included from age 8; children aged 2 and over may be included if they have lymphangiomatosis or an ADP-ribosylation defect, or have a family member with such a defect; other age exceptions may apply if specific approval is granted by the relevant review board (confirm with trial site).
- People who are not able to complete reliable breathing (pulmonary function) tests; healthy volunteers, patient relatives (except those connected to ADP-ribosylation defects), and asthma patients from Suburban Hospital must be between 18 and 90 years of age.
- For the bronchoscopy (a camera procedure to look inside the airways) part of the study specifically, people who have any medical reason that makes this procedure unsafe are not eligible.
- People whose illness is at an advanced stage where the risk of the bronchoscopy procedure is considered significant, even if there is no specific named reason to avoid it.
- People with an allergy to local anaesthetic agents such as lidocaine are not eligible for the bronchoscopy portion.
- People who currently have, or have recently had, a respiratory infection within the last 4 weeks are not eligible for the bronchoscopy portion.
- People who are pregnant or breastfeeding are not eligible for the bronchoscopy portion.
- People younger than 18 or older than 65 are not eligible for the bronchoscopy portion.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Joel Moss, M.D., National Heart, Lung, and Blood Institute (NHLBI)
Phone: (301) 827-1376
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
evaluating the role of hereditary factor
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.