sexually transmitted infections
Conditions
Interventions
None listed
Sponsors
Sapporo Medical University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Patients who have given consent for this study (ii) Patients for whom information on medical treatment and prognosis can be obtained from their medical records.
Exclusion criteria
Exclusion criteria: Patients who have requested not to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the minimum inhibitory concentration of antimicrobial agents against each bacterium as an antimicrobial susceptibility test. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints are the drug resistance mechanism and analysis by molecular type. | — |
Countries
Japan
Contacts
Public ContactMitsuru Yasuda
Sapporo Medical University School of Medicine Department of Infection Control & Laboratory Medicine
Outcome results
None listed