Study of the clinical utility of chlamydia pneumoniae detection using the LAMP method

Study of the clinical utility of chlamydia pneumoniae detection using the LAMP method - Study of the clinical utility of chlamydia pneumoniae detection using the LAMP method

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000027444

Enrollment

325

Registered

2017-05-22

Start date

2016-05-02

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

Chlamydia pneumonia

Interventions

Clinical performance test

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with bronchitis or pulmonary inflammatory symptoms suspected of atypical pathogen infection

Exclusion criteria

Exclusion criteria: Use of prohibited drugs Macrolide tetracycline New quinolone

Design outcomes

Primary

Measure	Time frame
Consistency of results of PCR method and test of antibody titer method and LAMP method	—

Countries

Japan

Contacts

Public ContactHiroto Akaike

Kawasaki Medical School pediatrics

redpond@med.kawasaki-m.ac.jp086-462-1111

Outcome results

None listed

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