NCT00499187已完成不适用
A Preliminary Evaluation of Fanconi Syndrome Due to Antiretroviral Therapies in HIV-Infected Persons
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 56
- 试验地点
- 1
- 主要终点
- Time to TDF discontinuation after diagnosis of Fanconi syndrome
研究概览
简要总结
Cross-sectional cohort study of participants with HIV with or without protocol-defined Fanconi syndrome (confirmed creatinine clearance [CLcr] decline and evidence of proximal tubulopathy).
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Time to TDF discontinuation after diagnosis of Fanconi syndrome
时间窗: Up to 48 weeks
Time to confirmed resolution of Fanconi syndrome
时间窗: Up to 48 weeks
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
相似试验
Unknown
不适用
Genotyping FcɣRs Genes of HIV-1 Patients "Progressor": Correlation With the Changing Profile of the InfectionHIV InfectionNCT03130296University Hospital, Strasbourg, France230
已完成
不适用
The Asia Pacific NeuroAIDS Consortium (APNAC) StudyHIVHIV-related neurological diseasesInfection - Acquired immune deficiency syndrome (AIDS / HIV)Neurological - Other neurological disordersACTRN12605000493640ational Institute of Mental Health and National Institute of Neurological Disorders and Stroke600
Enrolling By Invitation
不适用
Prevalence of Advanced Fibrosis in Patients Living With HIVFatty Liver DiseaseNCT04066608Johannes Gutenberg University Mainz300
已完成
不适用
An Observational Study of Distress, Immune Function, and Pain in HIV.Chronic PainHIVDistress, EmotionalImmune System and Related DisordersCentral SensitisationNCT04757987University of Cape Town107
已完成
4 期
ROCKET II - Randomized Open Label Switch for Cholesterol Elevation on Kivexa + Kaletra Evaluation TrialHIV-1NCT00772902Gilead Sciences85