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Scientists investigate link between asthma and severe RSV infections
NCT ID NCT01224691
First seen Jun 24, 2026 · Last updated Sep 01, 2026 · Updated 9 times
Summary
This study examined whether a chemical called TGF-Beta, which is more common in the lungs of people with asthma, makes them more vulnerable to respiratory syncytial virus (RSV). Researchers collected lung cells from 113 healthy adults and mild asthmatics using a bronchoscopy. The goal was to understand the biological reasons behind increased RSV susceptibility in asthma, which could guide future treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could point toward new treatments to protect people with asthma from severe RSV infections.
- What could go wrong
- This is an observational study, not a treatment trial. It is small and early-stage, so findings may not lead to direct therapies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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113 people
The number who actually took part.
- Started
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Mar 2012
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants will be individuals from the Research Triangle Park (RTP) area in North Carolina (see Section 6.2.1 for Recruitment Methods). Participants will be between the ages of 18 and 60 years and will be 1) healthy non-asthmatics and 2) mild asthmatics defined by 2008 Global Initiative for Asthma (GINA) criteria.@@@
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
-INCLUSION CRITERIA: 1. Male or female between 18 and 60 years of age 2. Non-asthmatics and mild asthmatics as defined below: * Non-asthmatic must have no prior diagnosis of asthma, no history of health care utilization or medication use for asthma, no current symptoms, and Forced Expiratory Volume in 1 Second (FEV1) greater than or equal to 80% predicted. * Asthmatics must have physician-diagnosed asthma for at least one year and evidence of mild, persistent disease during the month prior to Visit 1 (based on 2008 GINA guidelines). a) Participants who are currently taking a controller medication must: i. use the equivalent to GINA Step 1 or 2 therapy; and ii. have controlled disease, as defined by: * daytime symptoms less than or equal to 2 times week, such as wheezing, tightness in the chest, shortness of breath, and cough, * no nocturnal symptoms; b) Participants who are not currently taking a controller must have: i.\<TAB\>daytime symptoms \> 1 time a week but \< 1 time a day, such as wheezing, tightness in the chest, shortness of breath, and cough; ii. nocturnal awakenings \> 2 times a month but \< 1 time a week; c) All asthmatic participants must have either: i.\<TAB\>Pre-bronchdilator FEV1 greater than or equal to 80% predicted and a positive methacholine challenge (PC20 less than or equal to 4 mg / ml); or ii.\<TAB\>Pre-bronchodilator FEV1 \< 80% and post-bronchodilator FEV1 greater than or equal to 80% with significant bronchodilator reversibility (at least 12% or 200ml change in FEV1) 3. Participants must be able to understand and provide written informed consent 4. Participants must be able to travel to the CRU and the EPA EXCLUSION CRITERIA: 1. Use of oral steroid treatment(s) within 30 days of Visit 1 2. Acute asthma-related healthcare utilization within 30 days of Visit 1, such as ED visits, systemic corticosteroids, and nebulizer treatment for asthma exacerbation 3. Known or suspected respiratory infections within 30 days of Visit 1, such as flu, pneumonia, severe cold, tuberculosis, or bronchitis 4. Known or suspected viral infection within 30 days of Visit 1 5. History of chronic obstructive pulmonary disease other than asthma 6. History of immunological disease or current cancer 7. Uncontrolled cardiovascular disease such as angina, prior myocardial infarction, stroke, and high cholesterol 8. Cardiac malformations 9. Pulmonary hypertension 10. Bleeding disorders 11. Facial deformity, major facial surgery 12. Currently pregnant or breast feeding 13. Current smoker, significant second-hand smoke exposure (defined by urine cotinine \> 100 ng/ml at Visit 1 or Visit 2) or former smokers (defined by a history of smoking \> 100 cigarettes) 14. Insulin dependent diabetes 15. Used any of the following medications within 30 days of Visit 1: oral corticosteroids, systemic immunosuppressants or other immune-modifying drugs \[e.g., Rituxan, Humira, Enbrel, Azathioprine (Imuran), Cyclosporine (Neoral, Sandimmune, and SangCya), cyclophosphamide, TNF antagonists\], anticoagulants (clopidogrel, heparin, enoxaparin and related drugs, coumadin), and sustained use (i.e. more than one dose per day for more than two days) of non-steroidal anti-inflammatory drugs (aspirin, ibuprofen, indomethacin) within seven days of bronchoscopy 16. Allergy or history of adverse reactions to methacholine or lidocaine 17. Severe asthma as defined by a history of intubation for unstable asthma 18. Any condition that, in the investigator's opinion, places the participant at undue risk for complications (e.g. from PFTs, fiberoptic bronchoscopy, bronchalveolar lavage and/or bronchial brushings) 19. Temperature \> 37.6 C; blood pressure \< 90/50 mm Hg or blood pressure \>170/95 mm Hg; pulse rate \< 50 or \> 100 beats/minute 20. Body weight \< 50 kg (\<110 lbs) 21. The following abnormal lab values (values obtained during clinical assessment): * Platelet count \< 100,000 per 10(9)/L * White blood cells count \< 3000 per 10(9)/L * Hematocrit \< 35% for both female and male * Prothrombin Time (PT) / Abnormal International Normalized Ratio (INR) and partial prothromboplastin time (PTT) based on reference laboratory established reference ranges * Serum creatinine \> 1.4 mg/dL
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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NIEHS Clinical Research Unit (CRU)
Research Triangle Park, North Carolina, 27709, United States
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