Treatment Responses of Early Syphilis to Ceftriaxone Plus Doxycycline
Early Syphilis
About this trial
This is an interventional treatment trial for Early Syphilis
Eligibility Criteria
Inclusion Criteria: PLWH aged 20 years or more PLWH with early syphilis (i.e. primary, secondary, or early latent syphilis), confirmed by a positive rapid plasma reagin (RPR) titer with a reactive Treponema pallidum particle agglutination (TPPA) assay. PLWH has provided informed consent Exclusion Criteria: PLWH with RPR titers of less than 4 Exposure to antibiotics with activity against T. pallidum, such as penicillins, third- generation cephems, doxycycline, or macrolides, within the preceding 4 weeks A known or suspected infection other than syphilis requiring additional treatment with an antimicrobial active against T. pallidum A history of intolerance to penicillin, ceftriaxone, or doxycycline Pregnancy
Sites / Locations
- Kuan-Yin LinRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
single-dose ceftriaxone plus doxycycline
single-dose BPG plus doxycycline
single-dose ceftriaxone (1g intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days)
single-dose BPG (2.4 MU intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days)