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Clinical study of Ganoderma lucidum extract in the treatment of motor and non motor symptoms in patients with early PD

Clinical study of Ganoderma lucidum extract in the treatment of motor and non motor symptoms in patients with early PD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100005251
Enrollment
Unknown
Registered
2021-08-28
Start date
2021-09-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Parkinson's disease

Interventions

placebo group:Randomly into group
Treatment group, :Randomly into group

Sponsors

Xuanwu Hospital of Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: A) Meets the diagnostic criteria of "clinically probable PD" for primary Parkinson's disease of MDS; B) Age 30-80 at diagnosis of Parkinson's disease; C) H-Y clinical grade =2; D) UPDRS H2o between 10 and 30 points (10 and 30 points); E) The course of disease does not exceed 5 years; F) Is not receiving anti-Parkinson's drugs or other treatment, or has been discontinued for more than 2 weeks (including dopamine preparations, dopamine agonists, COMT inhibitors, MAO inhibitors, antan, amantadine); G) Agree to participate in this study, sign the informed consent, abide by the relevant experimental regulations, take medication on time and come for regular review; H) Agree to be treated only with experimental drugs for the next 1.5 years, and to take anti-Parkinson's drugs as prescribed if necessary.

Exclusion criteria

Exclusion criteria: A) Patients with atypical or secondary Parkinson's disease; B) A history of psychiatric symptoms or mental illness; C) Cognitive impairment (MDSE =24); D) Participating in other drug trials within the past 3 months; E) Severe liver and renal function abnormalities (more than 3 times the normal mean); F) ongoing use of anti-Parkinson's drugs; G) Not to sign the informed consent

Design outcomes

Primary

MeasureTime frame
MDS-UPDRS;

Secondary

MeasureTime frame
Parkinson's Syndrome Scale of Chinese medicine;ADAS-cog;Parkinson's sleep scale;Olfactory Argentine Questionnaire;Depression Scale GDS-30;ROME?;MMSE&MoCA;Parkinson's Pain assessment Scale;Schwab-England Disability Scale;

Countries

China

Contacts

Public ContactLi Jun

The First Affiliated Hospital of Anhui University of Chinese Medicine

18788899199@qq.com18788899199

Outcome results

None listed

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