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临床试验/NCT02065986
NCT02065986已完成4 期

Pre-exposure Option for Reducing HIV in the UK: an Open-label Randomisation to Immediate or Deferred Daily Truvada for HIV Negative Gay Men.(PROUD)

MRC [ycm]1 个研究点 分布在 1 个国家目标入组 544 人开始时间: 2012年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
544
试验地点
1
主要终点
Time to accrual of 500 participants and Retention at 12 and 24 months from randomisation

研究概览

简要总结

This study is looking at a new way to reduce the risk of catching HIV - Truvada-PrEP.

To find out whether a daily tablet, Truvada, can safely reduce the risk of gay men catching HIV, we need to do a large trial in which half the men do not receive Truvada for one year. We do not know if gay men at risk of HIV are interested in taking Truvada, and if they are, whether they would be willing to wait a year before they can take it. The reason it may not be safe, is that taking Truvada-PrEP may lead to an increase in risk behaviour. This could mean there was more chance of catching HIV and other infections.

As well as finding out if a large trial would be possible, this study will looks at other factors including:

  • Whether people using PrEP change the number of partners they have sex with
  • Whether people using PrEP change how often they use condoms
  • Whether PrEP leads to higher rates of other sexually transmitted infections (STIs).

This information on changes in sexual activity over time is one of the most important aspects of the study, because we have never collected this before in the UK. This means we don't know what happens to people's sexual activity without PrEP! In October 2014 an interim analysis of the PROUD study data showed that pre-exposure prophylaxis (PrEP) was highly protective against HIV for gay men and other men who have sex with men (MSM) at high risk of infection. The PROUD Trial Steering Committee announced that participants on the deferred arm of the study, who had not yet started PrEP, should be offered the opportunity to begin PrEP ahead of schedule. As a result, we changed the study design and offered all enrolled participants the opportunity to access PrEP. All study participants will be followed up until study closure in October 2016

详细描述

Intervention and control groups:

Arm A: Immediate offer of Truvada-PrEP Arm B: Deferred (12m) offer of Truvada-PrEP

Method of randomisation:

Randomisation will be performed centrally using a computer algorithm based on random permuted blocks stratified by site.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Born to male gender, age 18 years or more
  • Previously attended the enrolling clinic on at least one occasion
  • Completed a screen for HIV and STIs
  • HIV negative by a routinely used assay within 4 weeks prior to or on the day of randomisation
  • Reported unprotected anal intercourse (UAI) on more than one occasion within the 90 days prior to randomisation
  • Likely, in the opinion of the volunteer, to have UAI in the next 90 days
  • Willing and able to comply with the visit schedule throughout the follow-up period
  • Willing and able to provide written informed consent

排除标准

  • An acute viral illness that could be due to HIV seroconversion
  • Any contraindications to Truvada according to the current package insert
  • Treatment for hepatitis B infection indicated or ongoing
  • Unlikely, in the opinion of the clinician, to comply with the randomised allocation

研究组 & 干预措施

Arm A: Immediate offer of Truvada-PrEP

Experimental

Immediate offer of Truvada (once daily tablet containing 300mg tenofovir disoproxil (TDF) and 200mg of emtricitabine (FTC)

干预措施: Truvada (once daily tablet containing 300mg tenofovir disoproxil (TDF) and 200mg of emtricitabine (FTC) (Drug)

Arm B: Deferred (12m) offer of Truvada-PrEP

Other

Access to Truvada from 12 months after enrolment

干预措施: Truvada (once daily tablet containing 300mg tenofovir disoproxil (TDF) and 200mg of emtricitabine (FTC) (Drug)

结局指标

主要结局

Time to accrual of 500 participants and Retention at 12 and 24 months from randomisation

时间窗: 2 years

次要结局

  • HIV infections acquired between trial entry and 12 months, and between 12 and 24 months(24months)

研究者

发起方
MRC [ycm]
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

MRC [ycm]

Medical Research Council

Medical Research Council

研究点 (1)

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