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临床试验/NCT00285883
NCT00285883已完成3 期

Directly Observed Therapy in High Risk Populations in Newark, NJ

Saint Michael's Medical Center2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2004年4月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
30
试验地点
2

研究概览

简要总结

30 patients with poor antiretroviral therapy compliance will be identified from our pool of patients at Saint Michael's Medical Center and be given Directly observed therapy.

详细描述

30 patients with poor antiretroviral therapy compliance will be identified from our pool of patients at Saint Michael's Medical Center. Consent will be obtained, their regimens will be switched to QD based on previous therapies and resistance patterns if available. Patients will be placed on direct observed therapy.Each patient will be placed on Fortovase/Ritonavir (1600mg/100mg)QD plus two or three NRTIs based on a phenotypic baseline testing to a protease inhibitor. Patients will visit the office at baseline, weeks 1, 4, 8, 12, 16, 24, 32, 40, and 48. Patients will also be visited daily by the social worker (or designee) to observe patients taking their antiretroviral therapy for 6 months. After six months of direct observed therapy patients will be given a diary card to record administration of medications and the social worker ( or designee) will visit the home twice weekly. If the patient experiences a change in therapy secondary to virologic failure, the patient will return to baseline visit for the new once a day regimen. Virologic failure will be defined as < .5 log drop between each visit or > 400 copies/mL at week 24 on two separate occasions at least 14 days apart

研究设计

研究类型
Interventional

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

  • Men and Women > 18 years of age with a confirmed HIV-1 diagnosis
  • CD4 count <350 and or history of opportunistic infection
  • HIV PCR >55000 and >55,000 on one occasion in last 12 months
  • Patients with poor compliance (Poor compliance will de defined as taking less than 80 percent of prescribed medication
  • Patients with mental illness, HIV dementia, substance abuse or social factor prohibiting compliance
  • Willingness to sign informed consent or legal guardian

排除标准

  • ALT/AST > 5X ULN
  • CReatinine >2.0 -

研究者

申办方类型
Other

研究点 (2)

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