PACTR202302499607694尚未招募4 期
Delivery of Cabotegravir LA Injectable pre-exposure prophylaxis (PrEP) as an HIV prevention product option within the Fast-PrEP project.
Desmond Tutu Health Foundation0 个研究点目标入组 1,800 人开始时间: 2023年2月14日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 1,800
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 13 Year(s) 至 18 Year(s)(—)
- 性别
- All
入选标准
- •Aged 15-29 years
- •Member of a target population: adolescent girls and young women, young key populations (young people who trade sex; young gender and sexually diverse populations), or intimate partners of these populations.
- •Pregnant and breastfeeding women
- •HIV negative
- •Body weight >= 35 kg at baseline
- •Currently residing in the study criteria
- •Able to provide written, informed voluntary consent to partake in the study and willing
- •Able to receive a PrEP product
排除标准
- •Confirmed HIV-positive test result and/or signs and symptoms of an acute HIV infection
- •Weight <35kg
- •Clinical conditions - pregnant women cannot use the vaginal ring; individuals with inflammatory skin conditions that could compromise the safety of an intramuscular injection.
- •Allergy to any of the study products
- •Use of contraindicated medications (e.g. Rifampicin should not be co-administered with CAB-LA).
- •Do not spend a reasonable amount of time in the study area as residents, for school, or work, or are otherwise unable to participate in study visits for geographical reasons, according to the site investigator
- •Medical, social or other condition that, in the opinion of the site investigator, would interfere with the conduct of the study or safety of the participant (e.g., provided by self-report, or found upon medical history and examination or in available medical records)
研究者
相似试验
尚未招募
不适用
Injectable cabotegravir and rilpivirine Observational Study in Australian tertiary and primary care settings. A Cohort Study. (ICAROS)ACTRN12623000281695Prahran Market Clinic300
已完成
不适用
A Phase 1, Open-label, Single Intravenous Infusion Dose Study to Evaluate the Mass Balance, Pharmacokinetics, Metabolism, and Excretion of TAK-954 Containing Microtracer ([14C]-TAK-954)in Healthy Male SubjectsNL-OMON46703Millennium Pharmaceuticals Inc6
已完成
3 期
Pre-incisional bupivacaine infiltration trocarincions, reduction of postoperative pain?pijnbelevingincisional pain1006291510041297NL-OMON30342Ikazia Ziekenhuis100
进行中(未招募)
不适用
Preoperative administration of controlled-release oxycodone vs morphine as transition oppioid for TIVA in pain control post VATS - NDPatients subjects at VATS for spontaneus pneumothoraxMedDRA version: 9.1Level: LLTClassification code 10062043Term: Lung operationEUCTR2008-002662-56-ITAZIENDA OSPEDALIERA DI PARMA
尚未招募
Unknown
A clinical study to determine the safety and performance of Everads Injector for Injection of triamcinolone acetonide in suprachoroidal space of eye.CTRI/2024/01/061410Everads Therapy Ltd.
