Anthrax secrets revealed: new study tracks infection and vaccine response
NCT ID NCT00050310
First seen Jun 27, 2026 · Last updated Sep 17, 2026 · Updated 15 times
Summary
This study follows people who have or had anthrax, those exposed, and healthy vaccinated volunteers to learn how the body fights the disease. Researchers will track symptoms, immune responses, and long-term health for up to 2 years. The goal is to better understand anthrax and improve future treatments and vaccines.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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15 people
The number who actually took part.
- Started
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Oct 2002
- 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
Individuals who have recovered from anthrax infection. Cohorts are based on route of infection.
- Ages
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3 to 100 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: Subjects at least 3 years old, including pregnant women, are eligible for inclusion if they meet one of the five criteria listed below, are hemodynamically and clinically stable, and agree to stored samples. Women of child-bearing age or potential will not be excluded from participation but pregnancy status will be determined by serum or urine pregnancy test at time of enrollment in order to optimize subsequent evaluation and care. Although the study is open to participants at least 3 years old, pediatric anthrax cases are historically rare and essentially of the cutaneous type. Therefore, few, if any pediatric subjects are expected. Decisionally impaired subjects will be included in this study only if a Legally Authorized Representative (LAR) understands and is willing to sign a written informed consent document. 1. Inhalation Anthrax (acute or recovering infection) CONFIRMED: --nonspecific febrile illness followed by sepsis and/or respiratory failure AND --B anthracis isolation (via culture) from any site OR 2 supportive lab tests OR SUSPECTED: --nonspecific febrile illness followed by sepsis and/or respiratory failure with no alternative diagnosis AND --one supportive lab test OR direct epidemiological link to a confirmed environmental exposure 2. Cutaneous Anthrax (acute or recovering infection) CONFIRMED: --characteristic lesion (papule-\>vesicular-\>depressed black eschar plus or minus edema, erythema, necrosis, or ulceration) AND --B anthracis isolation (culture) from any site OR 2 supportive lab tests SUSPECTED: --Characteristic lesion with no alternative diagnosis AND --one supportive lab test OR direct epidemiological link to a confirmed environmental exposure 3. Gastrointestinal Anthrax (acute or recovering infection) CONFIRMED: --Severe abdominal pain often associated with bloody vomiting/diarrhea followed by fever/septicemia AND --B anthracis isolation (culture) from any site OR 2 supportive lab tests SUSPECTED: --Severe abdominal pain often associated with bloody vomiting/diarrhea followed by fever/septicemia with no alternative diagnosis AND --1 supportive lab test OR direct epidemiological link to a confirmed environmental exposure These definitions were subsequently updated by the CDC in 2010 to accept clinically compatible symptoms plus one of the following: a positive culture, a positive immunohistochemical stain for antigen, a 4-fold increase in anti-PA IgG or a positive documented exposure with detection of DNA via PCR (26). 4. Exposed individuals who are clinically asymptomatic. 5. Past or imminent vaccination in healthy (non-anthrax exposed). 6. Hemodynamically and clinically stable at time of evaluation at NIH. * Hemodynamically: stable vital signs * Clinically: no obvious signs of disease progression (e.g. worsening pleural effusions or increasing cutaneous edema) * acute/newly recovered patients must be receiving standard antimicrobial therapy 7. Participant agrees to stored samples. EXCLUSION CRITERIA: Inability of subject or Legally Authorized Representative (LAR) to understand or subject not willing to sign a written informed consent document.
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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
More trials for these conditions
Other studies related to the condition(s) this trial covers.