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Clinical Trials/NCT05094635
NCT05094635UnknownNot Applicable

Characteristics of Immunogenicity Against SARS-CoV-2 in the Community With Home-quarantined Covid-19 Patients in Ho Chi Minh City, Vietnam

University of Medicine and Pharmacy at Ho Chi Minh City1 site in 1 country772 target enrollmentStarted: November 30, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
772
Locations
1
Primary Endpoint
SARS-CoV-2 anti-RBD IgG concentration

Study Overview

Brief Summary

This study will investigate the presence of SARS-CoV-2 neutralizing antibody and its association with demographic information, medical history of SARS-CoV-2 infected individuals, exposure history of close contacts, vaccination status, and compliance with the strategies for self-quarantine to prevent the transmission in the community where SARS-CoV-2 infected individuals were home-quarantined and treated.

Detailed Description

In the 4th outbreak of the covid-19 pandemic in Ho Chi Minh City since 27 April 2021, asymptomatic or mild covid-19 patients were self-quarantined and treated at home. This home care setting could yield risk of SARS-CoV-2 transmission from the index cases to the people living surroundings. Therefore, this study will be performed to investigate the immunogenicity against SARS-CoV-2 in household members or people lived in the same municipality with home-quarantined covid-19 patients.

All people over 18 years old, living in 2 blocks (V and Y) of Ngo Gia Tu apartment, which is located in District 10, Ho Chi Minh City, will be recruited into this study. A survey will be conducted using a questionnaire to collect the data related to the basic demographic information, medical history of SARS-CoV-2 infected individuals, exposure history of close contacts, vaccination status, and compliance with the strategies for self-quarantine to prevent the transmission in the community.

At the time of recruitment, Covid-19 rapid antigen detection tests using nasopharyngeal swabs will be performed for all study subjects. In addition, a total of 5mL of intravenous blood samples will be collected for serum extraction and DNA isolation. SARS-CoV-2 neutralizing antibody levels in serum samples will be evaluated by a surrogate virus neutralization test by using NeutraLISA kit® (Euroimmun, Luebeck, Germany). DNA will be isolated and stored for further use in investigating the association of ACE2 genetic polymorphisms with the prevalence of SARS-CoV-2 neutralizing antibodies.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • People who lived in the two blocks (V and Y) of Ngo Gia Tu apartment, located in District 10, Ho Chi Minh City, Vietnam, from July to September 2021
  • 18 years of age and older
  • Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria

  • People who were diagnosed with primary or secondary immunodeficiencies induced by diseases or medical treatments (immunosuppressants, chemotherapy, radiation therapy, ect.)

Outcomes

Primary Outcomes

SARS-CoV-2 anti-RBD IgG concentration

Time Frame: Up to 1 week after examination

SARS-CoV-2 anti-RBD IgG antibody concentration was reported after analysing the specimen

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University of Medicine and Pharmacy at Ho Chi Minh City
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lan Ngoc Vuong

Head of Department of Obstetrics and Gynaecology; Dean, Faculty of Medicine

University of Medicine and Pharmacy at Ho Chi Minh City

Study Sites (1)

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