Human Papillomavirus Infection Clinical Trial
Official title:
SEARCH Thailand and Thai Red Cross AIDS Research Centre
Verified date | April 2022 |
Source | Thai Red Cross AIDS Research Centre |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
1. To determine the prevalence and incidence of anal HSIL and associated risk factors among MSM who initiate ART during AHI.
Status | Active, not recruiting |
Enrollment | 100 |
Est. completion date | October 2024 |
Est. primary completion date | December 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Age 18 years or above. 2. Born biological male. 3. Self-identifies as MSM or transgender woman. 4. Enrolled in the SEARCH010/RV254 cohort. 5. In the stage of acute HIV infection diagnosed within 7 days (Fiebig I-V). 6. Agrees to start ART during acute HIV infection. 7. Had sex with a male partner at least once in the previous 3 months 8. Consents to participate in the study Exclusion Criteria: 1. Any history of previous HSIL diagnosis or treatment. |
Country | Name | City | State |
---|---|---|---|
Thailand | The Thai Red Cross AIDS Research Centre | Pathum Wan | Bangkok |
Lead Sponsor | Collaborator |
---|---|
Thai Red Cross AIDS Research Centre | amfAR, The Foundation for AIDS Research, South East Asia Research Collaboration with Hawaii, TREAT Asia |
Thailand,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The prevalence and incidence of anal HSIL among MSM who initiate ART during AHI will be lower than among chronically-infected HIV-positive MSM, Anal HSIL is diagnosed based on histology specimen and cytology (2001 Bethesda system) | The prevalence of anal HSIL and the incidence of anal HSIL during the follow-up period. Anal HSIL is diagnosed based on histology specimen. A composite anal HSIL outcome (including both cytologic HSIL/ASC-H and histologic HSIL) will also be used.
Incidence of HSIL during the follow-up period will be calculated as the number of new diagnoses per person time at risk. 95% confidence intervals (CI) will be calculated assuming a Poisson distribution. Cox proportional hazards regression will be used to identify factors associated with incident HSIL. |
12 months |
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