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临床试验/NCT03198884
NCT03198884已完成不适用

A Retrospective Study to Evaluate the Safety and Efficacy of a Nucleoside-Sparing Regimen of Darunavir, Ritonavir, and Dolutegravir

Southern Illinois Healthcare Foundation0 个研究点目标入组 20 人开始时间: 2017年1月1日最近更新:
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试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
主要终点
Number of Participants With RNA <50 Copies/mL at 48 Weeks

研究概览

简要总结

A Retrospective Study to Evaluate the Safety and Efficacy of a Nucleoside-Sparing Regimen of Darunavir, Ritonavir, and Dolutegravir

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

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

入选标准

  • ≥18 years old
  • Received a regimen of darunavir 800 mg/ritonavir 100 mg in combination with dolutegravir 50 mg QD for ≥24 weeks as documented in EMR
  • Laboratory reports (CD4, viral load, SrCr) available at time points +/- 4 6 weeks from 12, 24, 36, 48 weeks from start of regimen
  • Resistance data (if applicable)

排除标准

  • Received a regimen of darunavir/ritonavir in combination with dolutegravir for <24 weeks duration
  • Patients receiving darunavir/ritonavir + DTG+NRTI's
  • Missing laboratory data in ≥2 study time points
  • Patients missing more than five doses over two weeks prior study visit

结局指标

主要结局

Number of Participants With RNA <50 Copies/mL at 48 Weeks

时间窗: 48 weeks

Our first primary endpoint evaluated the percent of study subjects with an RNA \<50 copies/mL at 48 weeks after initiation of the once daily two-drug regimen.

The Change in Serum Creatinine From Baseline to 48 Weeks.

时间窗: 48 weeks

A second primary endpoint was evaluating the change in serum creatinine from baseline to 48 weeks for all subjects.

次要结局

  • Analysis of Creatinine Clearance at Time Points 24, 36 and 48 Weeks.(48 weeks)
  • Change in Mean CD4+ Cell Count From Baseline.(48 weeks)
  • Incidence of Adverse Events.(48 weeks)
  • Number of Grade 1 Adverse Events Reported(48 weeks)
  • Number of Participants With RNA <50 Copies/mL at 24, 36, and 48 Weeks(48 weeks)

研究者

发起方
Southern Illinois Healthcare Foundation
申办方类型
Other
责任方
Principal Investigator
主要研究者

John Verna

Physician Assistant

Southern Illinois Healthcare Foundation

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