Actively Recruiting
Viral Infections in Healthy and Immunocompromised Hosts
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2026-05-05
1000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Background: \- Viral infections are an important cause of illness and death in hospitalized patients as well as outpatients. New strains of viruses may appear and infect both healthy people and those with weak immune systems. A better understanding of these new virus strains (such as SARS-CoV-2, the virus that causes COVID-19) may help to control and prevent these infections. In particular, some viral infections that are less problematic in healthy persons can be life threatening in persons with weak immune systems, and viruses may be able to evolve more rapidly in persons with weak immune systems and therefore develop resistance to existing treatments. Researchers are interested in collecting samples and information from otherwise healthy persons or persons with weak immune systems to study the effects of viruses and their development. Objectives: \- To collect samples and data from individuals who have been exposed to or have contracted viral infections. Eligibility: * Individuals of all ages who have been diagnosed with a viral infection are suspected to have a viral infection, or have been in close contact with someone with a suspected or actual viral infection that is of interest to investigators in the Laboratory of Infectious Diseases. * Healthy persons and persons with weak immune systems (immunocompromised individuals) are eligible to participate. Design: * Participants will be pre-screened to determine if they meet the eligibility criteria for the trial. * If eligible, evaluation may include a medical chart review, a history and physical examination, review of clinical reports from outside hospitals and laboratories, and review of tissue biopsies. * Study procedures may include collection of blood, urine, saliva, nasal fluid sampling, throat swabs, stool, and genital swabs. For participants who have specimens collected as part of their medical care (e.g. wound swabs, spinal tap, bronchoscopy, liver biopsy etc.), researchers may use leftover specimens from the clinical laboratory for testing. * Specimens may be collected up to 4 times per week during the first 2 weeks after enrollment, and then as many as 2 times per week for up to 2 years. Some participants may be asked to continue providing specimens if there is concern for relapse or recurrence of the infection. * Treatment is not offered under this study.
CONDITIONS
Official Title
Viral Infections in Healthy and Immunocompromised Hosts
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants of all ages are eligible.
- Patients 2 years or older can enroll at the Clinical Center.
- Patients under 2 years old may enroll only remotely and will not visit the Clinical Center.
- Persons diagnosed with or suspected of having a viral infection of interest to investigators.
- Persons who have been in close contact with someone with or suspected to have such a viral infection or who recently received a viral vaccine.
- Persons who had a recent viral infection of interest that has since cleared.
- Healthy adults 18 years or older who will serve as controls and can provide informed consent.
- Adults unable to provide initial consent may be enrolled following HRPP Policy 403 procedures.
- Only NIH employees or contractors working at NIH are eligible for the COVID-19 antibody cohort.
You will not qualify if you...
- Patients unable to safely undergo study procedures and tests.
- Patients unwilling to have samples collected and stored for future use.
- Healthy control participants under 18 years old.
- Decisionally impaired adults.
- Pregnant women.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
J
Jeffrey I Cohen, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
6
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