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OpenTrials
Recruiting

NCT Number: NCT05387304

A Follow-up Study of Asymptomatic Infections and Diagnosed Patients With Covid-19 in Shanghai

This study is to clarify the distribution characteristics, host and clinical characteristics, disease outcome and risk factors, changes of multiple organs such as cardiopulmonary function and changes in social and psychological indicators during long-term follow-up of omicron variant asymptomatic infections and diagnosed patients

Recruiting

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Ruijin Hospital

Shanghai, China

Location status: Recruiting

Location contact

Erzhen Chen, Ph D

PRINCIPAL_INVESTIGATOR

Guang Ning, Ph D

PRINCIPAL_INVESTIGATOR

Ying Chen, Ph D

CONTACT

[email protected]

+8613917403314

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • SARS-Cov-2-RNA positive
  • informed consent signed

Exclusion criteria

  • informed consent rejected

Treatment and study plan

Primary outcomes

  1. long-term outcomes,changes of clinical characteristic and social psychology

    Time frame: 10 years

    the 3rd,6th,9th month,average one year discharge from hospital

Study contacts

Contact information is provided by the study sponsor or research team.

Ying Chen, Ph D

CONTACT

[email protected]

+8613917403314

Sponsors and collaborators

Lead sponsor

Ruijin Hospital

Other

Registry information

Important dates

Study start
2022
Primary completion
2032
Study completion
2032
First posted
May 24, 2022
Registry last updated
May 24, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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