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Study for the Role of Butylphthalide in Delaying the progression of Parkinson's disease (PD), Vascular Parkinson's disease (VP) and Parkinsonism-plus syndrome (PPS)

Study for the Role of Butylphthalide in Delaying the progression of Parkinson's disease (PD), Vascular Parkinson's disease (VP) and Parkinsonism-plus syndrome (PPS)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023725
Enrollment
Unknown
Registered
2019-06-09
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-06-11

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

Conditions

Parkinson's disease (PD), Vascular Parkinson's disease (VP) and Parkinsonism-plus syndrome (PPS)

Interventions

PD-Placebo:Placebo
PD-Butylphthalide:Butylphthalide
VP-Placebo:Placebo
VP-Butylphthalide:Butylphthalide
MSA-Placebo:Placebo
MSA-Butylphthalide :Butylphthalide
PSP-Placebo:Placebo
PSP-Butylphthalide:Butylphthalide

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Parkinson's disease (PD) was clinically diagnosed according to the clinical diagnostic criteria of the International Society for Motor Disability (MDS) in 2015. (2) Complying with the diagnostic criteria of vascular Parkinson's syndrome proposed by Zijlmans et al. in 2004 and the diagnostic criteria agreed by experts in diagnosis and treatment of vascular Parkinson's syndrome formulated by Parkinson's Disease and Dyskinesia Group of Neurological Society of Chinese Medical Association in 2017; (3) Complying with the second edition of MSA diagnostic criteria revised by Gilman in 2008; (4) It conforms to the clinical diagnostic criteria of PSP formulated by Parkinson's Disease and Dyskinesia Group of Chinese Medical Association Neurological Society in 2016 and the PSP clinical diagnostic criteria of International Society for Dyskinesia (MDS) in 2017. The above diagnosis needs to be made by experienced neurologists and confirmed by two doctors. (5) Aged 18 to 80 years; (6) At least one year after the course of the disease was determined, and the life expectancy was greater than or equal to one year. (7) In the past three months, no drugs that may affect the progress of the disease, such as Rashaquilane and other confirmed drugs with disease modification, vitamin E, coenzyme Q10 and other drugs that may affect the progress of the disease, should be stopped for more than two weeks if the above drugs have been used; (8) No long-term history of taking coffee or smoking. If so, the above food should be stopped for more than 2 weeks for elution. (9) The patient has the ability to answer or cooperate with a series of scales or questionnaires involved in the study; he or her guardian can and will sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Secondary Parkinson's syndrome caused by toxins, drugs, metabolism, ischemic-hypoxic encephalopathy, etc. (2) Those who suffered from severe brain injury or complicated craniotomy within 5 years before admission; (3) Patients with severe systemic diseases (cardiopulmonary diseases), consciousness disorders, stroke, severe coronary heart disease, diabetes mellitus, liver and kidney diseases, severe visual and hearing impairment, etc., affect their life expectancy; (4) Complicated with intestinal diseases and mitochondrial diseases; (5) Those who had a history of intracranial hemorrhage in the past three months and could not use butylphthalide drugs; (6) Complicated with other serious diseases leading to cognitive impairment or with severe mental impairment; (7) Anaphylaxis or intolerance to butylphthalide (Enpipr) at present or in the past; (8) Researchers believe that visits and assistant examiners cannot be completed in accordance with the requirements of the research program.

Design outcomes

Primary

MeasureTime frame
the mean change of UPDRS score from baseline to 48 weeks(PD,VP);the mean change of UPDRS score from baseline to 48 weeks(MSA);the mean change of UPDRS score from baseline to 48 weeks(PSP);

Secondary

MeasureTime frame
PDQ-39;CGI;mNSS;MMSE;MoCA;Schwab England;SCOPA-COG;H&Y??;ESS;HAMD;HAMA;ADL;ROME III;

Countries

China

Contacts

Public ContactDennis Qing Wang

Zhujiang Hospital of Southern Medical University

wqdennis@126.com+86 13829734526

Outcome results

None listed

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