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A multi-center, controlled trial of doxycycline for the prevention of sexually transmitted diseases among men who have sex with men

A multi-center, controlled trial of doxycycline for the prevention of sexually transmitted diseases among men who have sex with men

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100747
Enrollment
Unknown
Registered
2025-04-15
Start date
2024-09-24
Completion date
Unknown
Last updated
2025-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Syphilis

Interventions

Drug intake group:Take 200mg of doxycycline within 24 hours of high-risk behavior. If the cumulative dose reaches 200mg per day, the drug will not be taken on the same day. After the cumulative weekly
Control group:Have syphilis/HIV test every three months.

Sponsors

Dermatology Hospital, Chinese Academy of Medical Sciences (Institute of Dermatology, Chinese Academy of Medical Sciences)
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 70 years. 2.Currently free from syphilis, HIV, or genital Chlamydia trachomatis infection. 3.Individuals assigned male at birth (AMAB) with a history of male-to-male sexual behavior (MSM), who have engaged in one or more of the following high-risk sexual practices within the past 6 months: (1)Engaged in unprotected anal intercourse (2)Had >=2 male sexual partners (3)Self-reported history of sexually transmitted infections (STIs) other than HIV (e.g., syphilis, genital herpes, gonorrhea, chlamydial infection, chancroid, or lymphogranuloma venereum) with documented treatment completion (4)Previous or current use of HIV pre-exposure prophylaxis (PrEP) or post-exposure prophylaxis (PEP), or ongoing participation in HIV prevention trials 4.No history of tetracycline antibiotic use within the preceding 3 months. 5.Absence of severe hepatic or renal dysfunction based on medical history, with no evidence of active hepatitis B or C virus infections. 6.Demonstrated understanding of study objectives, protocol design, and potential outcomes, with voluntary consent to participate through written informed consent.

Exclusion criteria

Exclusion criteria: 1.Severe allergies or allergies to tetracycline components. 2.Patients with severe chronic diseases, metabolic diseases (such as diabetes, etc.), neuropsychiatric disorders. 3.Sick or poor compliance.

Design outcomes

Primary

MeasureTime frame
Syphilis incidence;Chlamydia trachomatis infection incidence;Incidence of adverse events in the medication group;Loses visit rate;

Secondary

MeasureTime frame
HIV incidence;Detection rate of gonococcal drug resistance;Detection rate of chlamydia resistance;

Countries

China

Contacts

Public ContactQianqiu Wang

Dermatology Hospital, Chinese Academy of Medical Sciences (Institute of Dermatology, Chinese Academy of Medical Sciences)

wangqianqiunj@126.com+86 139 5192 1995

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026