Scientists track severe allergies to uncover hidden patterns
NCT ID NCT01164241
First seen Jun 26, 2026 · Last updated Sep 11, 2026 · Updated 15 times
Summary
This completed study followed 945 people, mostly children and young adults with severe eczema or related allergic conditions, along with their relatives. Researchers observed how these diseases progress over up to a year, using tests like allergy skin pricks, blood draws, and lung function tests. The goal was to better understand the natural history of severe allergic inflammation, not to test a new treatment.
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 study could provide insights into how allergic diseases progress, potentially guiding future treatments.
- What could go wrong
- This is an observational study, not testing a new treatment, so it won't directly improve health. Results may take years to translate into 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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945 people
The number who actually took part.
- Started
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Jul 2010
- 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
Referrals for severe, familial or atypical allergic disease from throughout the country and world-- either physician or self referrals.
- Ages
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2 to 80 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: * Subject or unaffected relatives must: 1. Be at least 2 years of age and less than or equal to 21 years of age at the time of enrollment and have documented history of severe allergic inflammation or hypersensitivity, that began in the first 5 years of life, that is moderate to severe, and with continued inflammation or recurrent flares in the preceding 3 months. Patients greater than 21 years of age with a history of disease in the first 5 years of life and/or, if in the opinion of the PI or AIs, the patient would be of interest to fulfill the objectives of the study. OR 2. Be 2-80 years of age with a known or suspected genetic or congenital disorder associated with severe allergic inflammation or hypersensitivity, as determined by the PI or AIs. OR 3. Be an a relative of a patient enrolled in the protocol. * Have a private physician to provide local continuity of care. * Provide a letter of referral, with copies of pertinent medical history and laboratory studies as indicated, from the prospective study participant s referring physician; this is not a requirement for healthy relatives. * Be willing to donate blood, buccal swabs, saliva, skin and nasal swabs for research and clinical studies and for storage to be used for future research and genetic testing; for unaffected relatives, be willing to donate blood and/or undergo allergy skin testing, in addition to having blood samples stored for future research and genetic testing. * Pregnant women or women who become pregnant are eligible to participate or continue participation on the study. Healthy Volunteer must: * Be at least 18 years old and no greater than 80 years old, and able to provide informed consent. 2\. Have no history of severe or recurrent allergic diseases or reactions. * Be willing to have samples stored for research and genetic testing. EXCLUSION CRITERIA: Any subject with any of the following criteria will be excluded: * Presence of conditions that, in the judgment of the investigator or the referring physician, may put the subject at undue risk or make them unsuitable for participation in the study. * Inability or refusal to undergo study procedures. * Inability to participate for the duration of the study. Any unaffected relative or healthy volunteer with any of the following criteria will be excluded: * Presence of conditions that, in the judgment of the investigator or the referring physician, may put the subject at undue risk or make them unsuitable for participation in the study. * Inability or refusal to undergo study procedures. * Inability to provide informed consent.
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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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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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