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NCT04383444 · ClinicalTrials.gov registry record

Surveillance of Individuals Following SARS-CoV-2 Infection

A clinical trial, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
18
Enrollment target

NCT04383444: Completed study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT04383444 is a clinical trial that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 18 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04383444 has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
18 participants
Enrollment target

Study Summary

Background: People who have had contact with a person with a known SARS-CoV-2 infection are being told to self-quarantine for 14 days. This is done to avoid potential virus spread. But the actual time it takes for a person to develop an infection after being exposed to the virus is not well known. The proper quarantine time could be less or more than 2 weeks. Researchers hope this study can be used to help improve public health guidelines for quarantines, social distancing, and returning to work after a possible SARS-CoV-2 exposure. Objective: To better understand how long it takes a person to develop (or not develop) an infection with the SARS-CoV-2 virus after they have had contact with a person who has a confirmed infection. Eligibility: NIH staff members age 18 and older who had recent contact with a person who has a SARS-CoV-2 infection Design: Participants will have 3 study visits at the NIH Clinical Center. They may be asked to have an extra visit depending on the test results at the third visit. At each visit, participants will give a blood and saliva sample. It will be used to test for SARS-CoV-2 antibodies. Their temperature will be taken. They will complete a short survey to collect data about possible COVID-19 symptoms. At the first visit only, they will also complete a survey that asks about their recent social contacts. Two types of nasal samples will be collected at each visit. These samples will be tested for the SARS-CoV-2 virus. 1. a swab will be inserted deep into the back of the nose and 2. a swab will be inserted to the middle of your nose. Participation lasts 3 to 4 weeks.

Primary Outcome

Correlate results of SARS-CoV-2 RT-PCR using various sample types, antibody assays, and culture.

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2020-07-07
Est. Completion 2022-02-10

What the finished NCT04383444 record still lists

NCT04383444 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 18 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT04383444 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04383444 about?

NCT04383444 is a clinical study titled "Surveillance of Individuals Following SARS-CoV-2 Infection". Background: People who have had contact with a person with a known SARS-CoV-2 infection are being told to self-quarantine for 14 days. This is done to avoid potential virus spread. But the actual time it takes for a person to develop an infection after being exposed to the virus is not well known. ...

What is the current status of trial NCT04383444?

This trial is currently completed. The enrollment target is 18 participants. The study started on 2020-07-07. Estimated completion is 2022-02-10.

Who is sponsoring clinical trial NCT04383444?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT04383444, the US trial registry maintained by the National Library of Medicine. NCT04383444 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.