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Effect of Early Oral Aspirin on Immune Reconstitution in HIV-1 Infected Patients: A Clinical Stud

Effect of Early Oral Aspirin on Immune Reconstitution in HIV-1 Infected Patients: A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120145
Enrollment
Unknown
Registered
2026-03-10
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

HIV infection

Interventions

Aspirin combined with ART Group:Oral aspirin (100 mg) administered daily in the morning, on the background of continuous antiretroviral therapy (ART), for a duration of 24 weeks.
Standard ART Group:Continuous antiretroviral therapy (ART) alone, without aspirin administration, for a duration of 24 weeks

Sponsors

Beijing Ditan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. HIV-1 infected patients with suboptimal immune reconstitution after receiving effective antiretroviral therapy (ART) for more than 4 years. 2. Confirmed HIV-1 infection, defined as positive HIV-1 antibody test by ELISA and confirmed by Western blot. 3. Aged 18 to 65 years (inclusive), regardless of gender. 4. Received initial treatment at this hospital, voluntarily participated and signed the informed consent form; 5. Good self-care ability and ability to comply with the study protocol.

Exclusion criteria

Exclusion criteria: 1. Severe hepatic or renal impairment (e.g., hepatitis, renal failure). 2. Bleeding diathesis, active peptic ulcer, or a history of peptic ulcer disease. 3. Concomitant use of other medications that affect the immune system or lipid levels (e.g., immunosuppressants). 4. Pregnant or lactating women. 5. History of allergy or hypersensitivity to aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs). 6. Recent severe complications or other concurrent diseases (e.g., cardiovascular disease). 7. Thrombocytopenia. 8. Current participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
CD4/CD8 ratio;HIV-1 Viral Load;CD4 T lymphocytes;

Secondary

MeasureTime frame
Laboratory indicators (blood routine, four items of coagulation function, blood lipids, liver function, kidney function);Immunological Parameters;

Countries

China

Contacts

Public ContactYaxian Kong

Beijing Ditan Hospital, Capital Medical University

yaxiankong@126.com+86 10 84322262

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026