Scientists probe COVID-19's attack on immune cells
NCT ID NCT04401436
First seen Jun 27, 2026 · Last updated Sep 11, 2026 · Updated 2 times
Summary
This study looked at how the virus that causes COVID-19 reduces the number of infection-fighting white blood cells (lymphocytes) in the blood. Researchers collected blood samples and medical records from 240 adults with or recovering from COVID-19. The goal was to learn more about the body's immune response and find clues for future treatments.
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
-
240 people
The number who actually took part.
- Started
-
May 2020
- Finished
-
Feb 2025
- Lead sponsor
-
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
COVID 19 positive and recovered patients from inpatient settings at the NIH CC and Georgetown University Medical Center, and the local community for COVID 19 recovered patients.
- Ages
-
18 to 99 years
- Sex
-
Anyone
- Healthy volunteers
-
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. Aged \>=18 years. 2. Diagnosis of COVID-19 via molecular assay or other commercial or public health assay. 3. Meets one of the following criteria for COVID-19: 1. Group A, mild clinical presentation: asymptomatic to oxygen requirements \<-4L nasal cannula (NC). 2. Group B, moderate clinical presentation: oxygen requirements \>4L NC to \<=50% fraction of inspired oxygen (FiO2) on high-flow oxygen devices. 3. Group C, severe clinical presentation: non-invasive ventilation with oxygen requirements \>50% FiO2 on high-flow oxygen devices, any other modality of non-invasive ventilation, or mechanical ventilation. 4. Group D, recovered: meets CDC criteria for discontinuation of transmission-based precautions and disposition of patients with COVID-19 in healthcare settings. Enrollment will occur at least 30 days after the above criteria were met. 4. Able to provide informed consent. EXCLUSION CRITERIA: Individuals meeting any of the following criteria will be excluded from study participation: 1. Documented history of hemoglobin from most recent blood draw \<7g/dL if known. 2. Any condition that, in the opinion of the investigator, contraindicates participation in this study.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Coronavirus disease 2019 are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
MedStar Georgetown University Hospital
Washington D.C., District of Columbia, 20007, United States
-
MedStar Health Research Institute: Washington Hospital Medical Center
Washington D.C., District of Columbia, 20010, United States
-
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.
- New ibuzatrelvir tablet put to the test in healthy volunteers
- Heart MRI study seeks answers for lingering COVID symptoms
- Heartburn and arthritis drugs tested against COVID-19
- Experimental drug leronlimab tested in 484 severe COVID-19 patients
- Pfizer launches study to track symptoms of COVID-19 and flu in real time