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Efficacy and safety of tenofovir disoproxil fumarate in the treatment of Parkinson's disease

Efficacy and safety of tenofovir disoproxil fumarate in the treatment of Parkinson's disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098658
Enrollment
Unknown
Registered
2025-03-12
Start date
2024-01-23
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Parkinson's disease

Interventions

Observation group:take tenofovir disoproxil fumarate
control:use basic drugs

Sponsors

The Fourth Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients with Parkinson's disease with Hoehn Yahr grade 1~2.5; 2.Aged 18-65 years; 3.Cognitive function is normal (MMSE score >= 24 points), and can independently complete relevant scale surveys; 4.Patients volunteer to be tested and sign informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients with Parkinsonism, essential tremor, stroke, epilepsy, and other well-diagnosed neurological disorders; or have undergone cranial surgery such as deep brain stimulation; 2.Patients with abnormal liver and kidney function (severe liver function abnormalities: ALT, conjugated bilirubin, AST, ALP, total bilirubin, one of which is greater than 2 times the upper limit of normal; Moderate to severe renal dysfunction: creatinine clearance <60ml/min); 3.Infected with chronic hepatitis B or AIDS (HIV-1 infection); 4.Severe depression, schizophrenia, other psychiatric disorders or drug dependence; 5.Other serious physical diseases such as heart, lung, liver, kidney disease, blood disease and malignant tumor; 6.Pregnant or lactating women and seniors over 65 years of age; 7.Allergy or other contraindications to the investigational drug; 8.Other conditions that, in the opinion of the investigator, are not suitable for participation in this clinical study;

Design outcomes

Primary

MeasureTime frame
Liver and kidney function;UPDRS, Unified Parkinson's Disease Rating Scale;

Secondary

MeasureTime frame
Serum phospholipid;NMSS, Non-Motor Symptoms Scale;

Countries

China

Contacts

Public ContactZhao Guohua

The Fourth Affiliated Hospital, Zhejiang University School of Medicine

gzhao@zju.edu.cn+86 579 89935025

Outcome results

None listed

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