Clinical evaluation of three rapid immunochromatographic tests for the diagnosis of dengue virus infection

Clinical evaluation of three rapid immunochromatographic tests for the diagnosis of dengue virus infection - Clinical evaluation of rapid tests for dengue

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000011314

Enrollment

150

Registered

2013-07-30

Start date

2012-06-29

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

Dengue fever

Interventions

evaluate three rapid tests by using whole blood

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: acute febrile illness

Exclusion criteria

Exclusion criteria: 48 hours passed after fever resolution fever sustains over 10 days

Design outcomes

Primary

Measure	Time frame
Sensitivity and specificity compared with the gold standards (PCR and ELISA)	—

Countries

Japan

Contacts

Public ContactYasuyuki Kato

National Center for Global Health and Medicine Division of Preparedness and Emerging Infections, Disease Control and Prevention Center

ykato@hosp.ncgm.go.jp03-3202-7181

Outcome results

None listed

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