Skip to content

Evaluation of immunochromatography test kit in genital chlamydia infections rapid test.

Evaluation of immunochromatography test kit in genital chlamydia infections rapid test. - Evaluation of rapid diagnostic test.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000009794
Enrollment
200
Registered
2013-02-01
Start date
2013-02-01
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

Sexually transmitted infections

Interventions

None listed

Sponsors

Juntendo University
Lead Sponsor
Kanto Chemical Co.,Inc.
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1)Suffers from sexually transmitted infections. 2)Getting the agreement of the clinical evaluation from patients or her agents.

Exclusion criteria

Exclusion criteria: 1)Typical symptom(i.e. yoghurt like secretion) is appeared clearly and is not need the diagnosis to use the test kit. 2)Patient for whom a clinical followup and a clear final diagnosis are judged to be difficult.

Design outcomes

Primary

MeasureTime frame
Compare performance of the new test kit with the traditional one, and evaluate the usefulness in clinical testing. 1)Evaluate the correlation between the new kit and traditional tests. 2)Evaluate the usefulness of the handling and the rapidity.

Countries

Japan

Contacts

Public ContactYasuhisa Terao

Juntendo University Obstetrics and Gynecology

yterao@juntendo.ac.jp03-3813-3111

Outcome results

None listed

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