EUCTR2014-002569-32-NL进行中(未招募)不适用
Biomedical interventions for HIV prevention in MSM in Amsterdam: a demonstration project
Academic Medical Center0 个研究点开始时间: 2015年4月29日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Male
入选标准
- •1.Male or transgender, age 18 years or more
- •3.Completed HIV and STI screening
- •4.HIV negative by 4th generation Elisa antigen/antibody test.
- •5.Willing and able to comply to project visit schedule and procedures
- •6.Willing and able to give written informed consent
- •7.Sufficient understanding of Dutch or English
- •AND at least one of the following:
- •1.One or more documented STI (urethral or anal chlamydia or gonorrhoea, primary or secondary syphilis) in the last 6 months (either at STI clinic or a documented infection diagnosed elsewhere)
- •2.UAI with casual partners in the last 6 months
- •3.Received PEP after sexual risk incident in the last 6 months
- •4.HIV positive partner with unknown or detectable viral load
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 350
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •1.Signs or symptoms of acute HIV infection1
- •2.Hepatitis B infection (i.e. HbsAg positive)
- •3.Creatinine clearing (using cockroft gault formula) < 60 ml/min
- •4.Hypersensitivity for one of the components of fixed combination tablet containing tenofovir and emtricitabine
- •5.Unlikely, in the opinion of the clinician, to comply with trial schedule
研究者
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