Gonorrhea Clinical Trial
Official title:
Superiority of On-demand Pre-exposure Prophylaxis Versus Post-exposure Prophylaxis on Using Doxycycline for Preventing Sexually Transmitted Infections in Men Who Have Sex With Men
The goal of this clinical trial is to compare the effectiveness of doxycycline taken for on-demand pre-exposure prophylaxis (DoxyODPrEP) and its post-exposure use (DoxyPEP) in preventing bacterial sexually transmitted infections (STI), including chlamydia, gonorrhoea, and syphilis among men who have sex with men (MSM). The main questions it aims to answer are: 1. Is DoxyODPrEP superior to DoxyPEP? 2. Are both regimens safe? 3. Does the MSM community accept the use of doxycycline to prevent bacterial STI? Participants will be asked to take doxycycline according to the study arm they are randomly assigned to, and attend regular clinical follow-ups during the 2-year observation period. Researchers will compare the bacterial STI incidences between the two groups to see if DoxyODPrEP is superior to DoxyPEP.
Status | Not yet recruiting |
Enrollment | 300 |
Est. completion date | March 2027 |
Est. primary completion date | October 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - has had sex with another male in the past six months - normally reside in Hong Kong - can communicate in written and spoken Chinese or English - willing and able to give written informed consent - being willing and able to attend scheduled study clinic visits - at risk of STI (had condomless sex with more than one man in the past 12 months, history of STI diagnosis in the past 12 months, inclination to have condomless sex, and other HIV-PrEP-eligible criteria) Exclusion Criteria: - Being allergic to tetracycline class medicines - Currently taking medications that are contraindicated with doxycycline - Using antibiotics for more than 14 days in the month preceding enrolment |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Stanley Ho Centre for Emerging Infectious Diseases | Sha Tin |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to the first episode of gonorrhoea after the enrolment visit | Time to the first episode of gonorrhoea after the enrolment visit | Months 1 to 24 | |
Primary | Time to the first episode of chlamydia after the enrolment visit | Time to the first episode of chlamydia after the enrolment visit | Months 1 to 24 | |
Primary | Time to the first episode of syphilis after the enrolment visit | Time to the first episode of syphilis after the enrolment visit | Months 1 to 24 | |
Secondary | Safety profile | Percentage of participants experiencing adverse events and the associated grades | Months 1 to 24 | |
Secondary | Acceptability of regimens | Percentage of participants accepted the regimen | Months 1 to 24 | |
Secondary | Retention | Percentage of participants remained during the follow-up period | Months 1 to 24 | |
Secondary | Time to the first episode of HIV after the enrolment visit | Time to the first episode of HIV after the enrolment visit | Months 1 to 24 |
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