drugset / Trial / NCT06069141
Comparisons of Treatment Responses of Early Syphilis to Benzathine Penicillin G With or Without Doxycycline
Recruiting
688 enrolled
National Taiwan University Hospital
Chi Mei Medical Hospital · collabFar Eastern Memorial Hospital · collabKaohsiung Medical University Chung-Ho Memorial Hospital · collabKaohsiung Veterans General Hospital. · collabNational Cheng-Kung University Hospital · collabNational Taiwan University Hospital Hsin-Chu Branch · collabTaipei Veterans General Hospital, Taiwan · collabTaoyuan General Hospital · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
This randomized controlled superiority study will be conducted during 2023-2025. The eligible participants are adult people living with HIV (PLWH) who are newly diagnosed with early syphilis. Participants will be randomized in a 1:1 ratio to receive single-dose benzathine penicillin G (BPG) (2.4 MU intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days) or single-dose BPG. The primary outcome is serologic response, defined as a decline of rapid plasma reagin (RPR) titer by 4-fold or greater, at week 24 and week 48; and the secondary outcomes include microbiologic response of syphilis and bacterial sexually transmitted infections (STIs) assessed by nucleic-acid amplification test (NAAT) at week 4.
Timeline
- Start
- 2024-01-01
- Primary completion
- 2027-12-31
- Completion
- 2028-12-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Doxycycline | Small molecule | 100 mg | Oral |
| Comparator | Benzathine Penicillin G | Unknown | 2.4e+06 iu | Intramuscular |