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Special Investigation - Efficacy/Safety Evaluation of Clarithromycin in Patients With Mycoplasma pneumoniae Pulmonary Infections

Special Investigation - Efficacy/Safety Evaluation of Clarithromycin in Patients With Mycoplasma pneumoniae Pulmonary Infections - Special Investigation of Clarithromycin in Patients With Mycoplasma pneumoniae Pulmonary Infections

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000011964
Enrollment
80
Registered
2013-10-04
Start date
2013-08-01
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

Pulmonary Infections

Interventions

None listed

Sponsors

Shigeru KOHNO
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Age: over 15 and under 49 years old (2) Location for treatment: outpatient (3) Patients with acute upper respiratory tract infection including acute bronchitis (Acute tonsilitis, acute Pharngitis) (4) Patient who has cough of strong persistent susceptibility, becomes insomnia at night (5) Patient who judged that the intensity of cough had not passed over a peak (6) After development of symptoms, the patient for less than three weeks (7) Patient who has a person of the same cough by the circumferences (8) Patient to whom expectoration can extract not pus-sputum but pharynx (9) Patients who do not agree to participate in this study

Exclusion criteria

Exclusion criteria: (1) Patients enrolled in entry of the study (2) Patients within 7days of CAM treatment (3) Patient who has condition in an improvement tendency by medication of other antimicrobial drugs (4) Patients whose diseases have taboo against the used antibiotics. (5) Patient with the patient or the past which has a chronic respiratory disease (6) Patient who has cough owing to foreign-body aspiration (7) Patient who has cough owing to gastroesophageal regurgitation (8) Patient who takes a medicine in an ACE inhibitor and has cough owing to it (9) Patient who has cough owing to it, cough asthma, atopic, the patient that has cough owing to allergic rhinitis (10) Patient who has cough owing to cardiac disease (11) Confirmed influenza virus infection. (12) Patient permitted the unusual shades, such as tuberculosis and a tumor, by the breast image inspection

Design outcomes

Primary

MeasureTime frame
Evaluation of adverse event, Rate of bacterial eradication

Countries

Japan

Contacts

Public ContactKoichi IZUMIKAWA

Nagasaki University Second department of internal medicine

koizumik@nagasaki-u.ac.jp095-819-7273

Outcome results

None listed

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