Efavirenz 400mg in Treatment-naïve Chinese HIV-infected Patients

Status Completed

Clinical Trial Summary

Evaluating the efficacy, pharmacodynamics, and safety of Efavirenz 400mg in treatment-naïve Chinese HIV-infected patients.

Clinical Trial Description

Treatment-naive HIV-infected patients are designed to enroll and receive efavirenz 400mg combined with tenofovir (TDF) and lamivudine (3TC) as initial antiretroviral regimens, and monitoring for 48 weeks, to evaluate efavirenz concentration, T-cell subsets, HIV RNA load, and neuropsychiatric tests with Hamilton depression scale (HAMD) and Pittsburgh sleep quality index (PSQI) at baseline, 4, 12, 24, 48 weeks. ;

Study Design

Related Conditions & MeSH terms

HIV-1-infection

Clinical Trial Details

NCT number	NCT04596488
Study type	Interventional
Source	Peking Union Medical College Hospital
Contact
Status	Completed
Phase	N/A
Start date	June 1, 2017
Completion date	December 30, 2019

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