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Clinical study of Garenoxacin on male non-gonococcal urethritis

Clinical study of Garenoxacin on male non-gonococcal urethritis - Clinical study of Garenoxacin on male non-gonococcal urethritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014994
Enrollment
50
Registered
2014-08-30
Start date
2014-09-16
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

Non-gonococcal urethritis

Interventions

Garenoxacin 400mg once daily p.o. 7days

Sponsors

Jikei university katsushika medical center,Department of urology
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Outpatients with non-gonococcal urethritis over 20 years old. Patients who undersutand the study and agree with written informed consent. Ptients agree that they do not have sexual intercourse without using condom during the period of clinical trial.

Exclusion criteria

Exclusion criteria: Patient with a history of allergies against fluoroquinolone. Patient with convulsive disorders like epilepsy or with a history of these deseases. Patients who have severe heart diseases including inchemic heart diseases or arrthythmia. Patient with diabetis mellitus. Patient with systolic blood pressure of patients below 90mmHg. Patient with myasthenia gravis.

Design outcomes

Primary

MeasureTime frame
Microbiological efficacy of GRNX against causative bacteria(mMycoplasma genitalium,Chlamydaia trachomatis,Ureaplasma urealyticum)is investigated in non-gonococcal urethritis.

Secondary

MeasureTime frame
To evaluate the clinical efficacies of GRNX to non-gonococcal urethritis

Countries

Japan

Contacts

Public ContactHiroshi kiyota

Jikei university katsushika medical center Department of urology

kiyota@jikei.ac.jp0336032111

Outcome results

None listed

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