Skip to content

Clinical study to evaluate the efficiency of specific antibody against SARS-CoV-2 for the purpose of its social implementation

Clinical study to evaluate the efficiency of specific antibody against SARS-CoV-2 - Clinical study to evaluate the efficiency of specific antibody against SARS-CoV-2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040744
Enrollment
5000
Registered
2020-06-16
Start date
2020-06-22
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients who are scheduled to be hospitalization to Yokohama City University Hospital and Yokohama City university medical center

Interventions

We examine how many patients who never be diagnosed as COVID-19 have NP antibody. In addition, we will examine the relationship between NP antibody and neutralizing activity in patients with subclinic

Sponsors

Yokohama city university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients scheduled to be admitted to Yokohama City University Hospital or Yokohama City University Medical Center (2) Patients over 6 years old (3) Patients living in Japan (4) Patients who can collect nasopharyngeal swab and collect blood. If the PCR test using saliva sample can be performed within the insurance medical care, it is allowed (5) Patients who have obtained sufficient explanation about the research content and agreed to the document in writing, or when the participant himself/herself does not have the responsibility for consent, the relatives with whom he/she lives become a delegate and obtain consent.

Exclusion criteria

Exclusion criteria: (1) Patients who are already hospitalized (2) Patients suspected to be infected with COVID-19 such as common cold symptoms, upper respiratory tract symptoms, 37.5 degrees or more (3) Patients who are thought to have an effect on consent ability, such as mental illness (4) Patients with a new coronavirus infection in the past (5) Other patients who the investigator determined to be unsuitable for study participation

Design outcomes

Primary

MeasureTime frame
Fixed-point and time-course prevalence of NP antibody in patients without any clinical symptoms related to SARS-CoV-2

Countries

Japan

Contacts

Public ContactMie Tsuchiya

Yokohama city university hospital Clinical trial support center

johney@yokohama-cu.ac.jp045-787-2800

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026