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Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Evaluation of rapid diagnostic test for RS virus and adenovirus infection - Evaluation of rapid diagnostic test for RS virus and adenovirus infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000034777
Enrollment
1000
Registered
2020-12-01
Start date
2018-11-01
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

respiratory syncytial virus (RSV) infection, adenovirus infection

Interventions

Sample collection, assay with test kit

Sponsors

Sekisui Medical Co., Ltd.
Lead Sponsor
Zama Children&#39
Collaborator
s Clinic, Ichikawa Children&#39
Collaborator
s Clinic, Abe Children&#39
Collaborator
s Clinic, Kobayashi International Clinic, Jichi Medical University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients that visit the medical institution during this study, and include the following conditions: 1) Patients with suspected RSV or Adeno virus infection based on symptoms. 2) Patients who agree to participate in this study.

Exclusion criteria

Exclusion criteria: 1) Patients who are difficult to obtain clinical samples from. 2) For any reason other than above, patients who were determined by doctor as being unfit to participate in this study.

Design outcomes

Primary

MeasureTime frame
Sensitivity, specificity and detection limit of rapid diagnostic test for RS virus and adenovirus infection—

Countries

Japan

Contacts

Public ContactYuta Maehara

Sekisui Medical Co., Ltd. Research & Development

yuta.maehara@sekisui.com03-3272-0677

Outcome results

None listed

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