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NCT01606826Completed

Severe Asthma Research Program

Source: ClinicalTrials.gov · Last updated 14 Aug 2026

Brief summary (registry, in English)

The mission of the SARP is to improve the understanding of severe asthma through integrated study of its clinical and biological features and to evaluate their changes over time. The ultimate goal of these efforts is to promote better treatments for severe asthma.

Status (registry)
Completed
Study type
Observational
Enrollment
1100 (estimated)
First submitted
24 May 2012
Start date
Oct 2012
Primary completion date
31 Jul 2026
Lead sponsor
Milton S. Hershey Medical Center
Diseases
Asthma
NCT number
NCT01606826

What you commit to

  • Study type: Observational
  • Planned participants: 1100
  • From Oct 2012 to the primary completion date, 31 Jul 2026
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently participating in an investigational drug trial for asthma therapies.
    • Healthy Controls:

Other illness

  • Other chronic pulmonary disorders associated with asthma-like symptoms, including (but not limited to) cystic fibrosis, chronic obstructive pulmonary disease, chronic bronchitis, vocal cord dysfunction (that is the sole cause of respiratory symptoms and at the PI's discretion), severe scoliosis or chest wall deformities that affect lung function, or congenital disorders of the lungs or airways,
  • History of premature birth before 35 weeks gestation,

Age

  • Smoking history \> 10 pack years if ≥30 years of age, or smoking history \> 5 pack years if \<30 years of age (Note: if a subject has a smoking history, no smoking within the past year),

Other

  • Pregnancy during the characterization phase,
  • Current smoking,
  • Unwillingness to receive an intramuscular triamcinolone acetonide injection,
  • Evidence that the participant or family may be unreliable or poorly adherent to their asthma treatment or study procedures,
  • Planning to relocate from the clinical center area before study completion,
  • Any other criteria that place the subject at unnecessary risk according to the judgment of the Principal Investigator and/or attending physician(s) of record, or

Who the study is looking for

  • Physician diagnosis of asthma,
  • Age 6 years and older
  • Evidence of historical reversibility, including either:
    • FEV1 bronchodilator reversibility ≥ 12%, or
    • Airway hyperresponsiveness reflected by a methacholine PC20 ≤16 mg/mL.
  • History of chronic diseases that affect the lungs,
  • A history suggestive of allergic rhinitis, eczema or chronic sinusitis,
  • An improvement in FEV1 of more than 12% following 4 puffs of albuterol,
  • Smoking history \> 10 pack years if ≥30 years of age, or smoking history \> 5 pack years if \<30 years of age, or any smoking within the past year,
  • Respiratory tract infection within the past 4 weeks,
  • Pregnancy,
  • History of premature birth (\<35 weeks).

Criteria the registry did not label

  • Asthmatic Patients:

Age in the registry: 6 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Brigham & Women's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Children's Hospital, Boston
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Cleveland Clinic
Coordinator of this site? Confirm its status
ClevelandUnited StatesUnknown status
University of Wisconsin - Madison
Coordinator of this site? Confirm its status
MadisonUnited StatesUnknown status
University of Pittsburgh
Coordinator of this site? Confirm its status
PittsburghUnited StatesUnknown status
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status
Washington University
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Wake Forest University Health Sciences
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.