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Clinical Trials in China / NCT06356662
Recruiting Phase 1

Tenofovir Disoproxil Fumarate in the Treatment of Parkinson's Disease

NCT06356662 · tracked via the Priya Life Science China tracker
Sponsor
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Phase
Phase 1
Started
2024-01-23
Last updated
2025-02-17

Condition(s) studied

Parkinson Disease

Investigational drug(s) / intervention(s)

Tenofovir Disoproxil Fumarate

Tenofovir Disoproxil Fumarate: take tenofovir disoproxil fumarate 300mg/d

Study summary

To evaluate the efficacy and safety of tenofovir disoproxil fumarate in the treatment of Parkinson's disease. The changes of motor symptoms and the occurrence of adverse reactions in early Parkinson's disease patients who took tenofovir disoproxil fumarate and did not take Tenofovir disoproxil fumarate at different time points were compared.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * 1: Parkinson's disease: Hoehn Yahr= 1 to 2.5 2: MMSE score≥24 Exclusion Criteria: * 1: essential tremor, stroke, epilepsy and other well-defined neurological disorders 2: Or have received deep brain stimulation and other brain surgery 3: Abnormal liver and kidney function 4: Infected with chronic hepatitis B or AIDS (HIV-1 infection) 5: Severe depression, schizophrenia, other psychiatric disorders or drug dependence 6: Other serious physical diseases such as heart, lung, liver, kidney disease, blood disease and malignant tumor 7: Pregnant or lactating women and seniors over 65 years of age 8: Allergy or other contraindications to the investigational drug

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Guohua Zhao Hangzhou Zhejiang Recruiting

More The Fourth Affiliated Hospital of Zhejiang University School of Medicine trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06356662 on ClinicalTrials.gov ↗ ← All trials in China