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Observational Study on the Reconstruction of Immune Function in HIV/AIDS Patients after combined antiretroviral therapy by Artesunate Tablets and Moxibustion

Observational Study on the Reconstruction of Immune Function in HIV/AIDS Patients after combined antiretroviral therapy by Artesunate Tablets and Moxibustion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015289
Enrollment
Unknown
Registered
2018-03-21
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acquired Immune Deficiency Syndrome

Interventions

Queue one:Antiviral treatment of western medicine + artesunate tablet
Queue two:Antiviral treatment of western medicine + moxibustion method

Sponsors

China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Between the ages of 18 and 65, male and female; 2) the HIV antibody positive, by Western Blot confirmed test proof; 3) HAART treatment time is more than 1 year, and plasma HIV loads < 50 copies/ml is more than 18 months; 4) CD4 + T lymphocyte count < 300 cells/ul, or compared to the baseline growth < 20%; 5) voluntary to participate in this study, signed informed consent.

Exclusion criteria

Exclusion criteria: 1) Serious opportunistic infection before entering the group is not controlled; 2) Within a month before into the group or other drugs is participating in clinical trials of patients; 3) Within a month before into the group of immune modulators therapy; 4) the WBC < 2 x 10^9/L, N <1.0 x 10^9/L, Hb < 90 g/L, PLT < 75 x 10^9/L, liver and kidney dysfunction, abnormal liver function refers to the AST/ALT or T-BIL reference cap of 2 or more times, kidney function abnormal creatinine clearance below normal); 5) combined hepatitis c, liver cirrhosis, syphilis patient; 6) pregnant or lactating women and women of childbearing age without adopting safe contraception.

Design outcomes

Primary

MeasureTime frame
Absolute Value of CD4+ cells;Immune Reconstruction Efficiency;

Secondary

MeasureTime frame
CD8+, CD45RA+, CD45RO+, CD4+CD28+, CD8+CD38+, CD4+CD38+;Cell proliferation and apoptosis: CD4+ki67+/CD4+, CD8+ki67+/CD8+, mitochondrial membrane potential;clinical symptoms;WHO quality of life scale;Viral load;

Countries

China

Contacts

Public ContactWang Jian

China Academy of Chinese Medical Sciences

62tiger@163.com+86 010-64039230

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026