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Study on rapid diagnostic reagent for Mycoplasma pneumoniae antigen detection reagent

Study on rapid diagnostic reagent for Mycoplasma pneumoniae antigen detection reagent - Study on rapid diagnostic reagent for Mycoplasma pneumoniae antigen detection reagent

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000032625
Enrollment
150
Registered
2019-11-30
Start date
2018-04-25
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

Mycoplasma pneumoniae infectious disease

Interventions

None listed

Sponsors

MIZUHO MEDY Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient applicable to following items. 1) The patient with fever and a cough as presenting symptom 2) Case patient of 1) and require testing the antigen or nucleic acid of Mycoplasma pneumoniae. 3) The patient who has agreed with the participation to this examination

Exclusion criteria

Exclusion criteria: Irrelevance patient is excluded in the judgement of doctor.

Design outcomes

Primary

MeasureTime frame
Correlative evaluation with results obt ained by PCR assay.

Secondary

MeasureTime frame
Correlative evaluation of Mycoplasma pneumoniae antigen rapid diagnostic test results in throat swab and nasopharyngeal aspiration specimen.

Countries

Japan

Contacts

Public ContactTomonori Arao

MIZUHO MEDY Co., Ltd. R&D Planning Dept.

arao@mizuho-m.co.jp0942-85-0303

Outcome results

None listed

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