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Clinical Study on Dihydroartemisinin Suppressing Inflammation and Immune Dysregulation in HIV-Infected Patients

Clinical Study on Dihydroartemisinin Suppressing Inflammation and Immune Dysregulation in HIV-Infected Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122718
Enrollment
Unknown
Registered
2026-04-16
Start date
2024-12-27
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

HIV

Interventions

DHA combined with ART treatment group (high-dose DHA group):High-dose DHA combined with ART intervention
DHA treatment group (not receiving ART):DHA(Dihydroartemisinin)
Conventional ART treatment group (INRs control group): ART(Antiviral Therapy) intervention
DHA combined with ART treatment group (low-dose DHA group):Low-dose DHA combined with ART intervention
Control group (did not receive ART):None

Sponsors

Beijing Youan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.DHA treatment INRs studies: (1) confirmed experimental diagnosis of HIV infection; (2) Age 18~65 years old; (3) Body weight 50~90 kg; (4) Meet the diagnostic criteria for poor immune reconstitution: continuous ART treatment for more than 2 years; Plasma HIV load less than 50 copies/ml for more than 1 year; CD4 T lymphocyte count less than 350 cells/µL or annual increase of less than 20% from baseline; (5) Good compliance, able to ensure regular follow-up and specimen collection; (6) Volunteer to participate in this study and sign the informed consent form. 2.Study of DHA treatment in HIV-infected individuals not receiving ART: (1) Confirmed laboratory diagnosis of HIV infection; (2) Age 18–65 years; (3) Weight 50–90 kg; (4) After routine ART adherence counseling, the participant temporarily does not receive ART; (5) Good adherence, able to attend regular follow-ups and sample collection; (6) Voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Presence of other acute or chronic somatic or mental disorders; (2) Poor ART adherence; (3) Use of immunosuppressants or immune modulators within 6 months prior to screening, as well as other medications that may affect this study; (4) Other situations where the investigator believes the participant is unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
CD4+ T cell count;T cell activation markers (CD38, HLA-DR);

Secondary

MeasureTime frame
HIV DNA reservoir level;Plasma HIV RNA viral load;Expression level of candidate genes;Incidence of adverse events;T cell subset distribution;

Countries

China

Contacts

Public ContactZhang Tong

Beijing Youan Hospital, Capital Medical University

zt_doc@163.com+86 10 8399 7162

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026