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テノホビル、エムトリシタビン(またはラミブジン)+ロピナビルの継続投与と、ラルテグラビル+ダルナビルへの切り替えの比較

基本情報

NCT ID
NCT01294761
ステータス
完了
試験のフェーズ
該当なし
試験タイプ
介入
目標被験者数
59
治験依頼者名
National Center for Global Health and Medicine, Japan

概要

The main objective of this clinical trial in randomizing HIV infected patients under good HIV control with tenofovir (TDF), emtricitabine (or lamivudine) plus lopinavir/ritonavir (LPV/r) into switching the regimen to raltegravir (RAL) with darunavir/ritonavir (DRV/r) or continuing the ongoing regimen to compare these two groups' estimated glomerular filtration rate (eGFR) is to investigate whether anti-HIV treatment that does not contain TDF or other reverse-transcriptase inhibitors (NTRI sparing regimen) can be protective of patients' renal functions and has the same virological efficacy in comparison with a standard treatment with TDF, or not.

対象疾患

HIV Infections

介入

Raltegravir, Darunavir/r(DRUG)

実施施設 (1)

国立健康危機管理研究機構国立国際医療センター

Shinjuku, Tokyo, Japan