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Clinical efficacy and related mechanism of Edaravone and dexborneol in the treatment of newly diagnosed untreated Parkinson's disease patients

Clinical efficacy and related mechanism of Edaravone and dexborneol in the treatment of newly diagnosed untreated Parkinson's disease patients

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056774
Enrollment
Unknown
Registered
2022-02-15
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

parkinson’s disease

Interventions

patient group:Edaravone and dexborneol
Healthy control group:Nil

Sponsors

nanjing brain hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: The subjects were mainly from the PD Clinic of the Affiliated Brain Hospital of Nanjing Medical University. They were 30-75 years old at the time of enrollment, with normal vision or corrected vision, normal hearing in both ears, and all were right-handed. Inclusion criteria for PD patients: ?Diagnostic criteria for PD patients meet the 2015 MDS diagnosis criteria for PD; ?Have not taken any anti-PD drugs at the first visit; ?HAMD=8 points.

Exclusion criteria

Exclusion criteria: Exclusion criteria: ?History of consciousness disturbance; ?Family genetic diseases; ?Central nervous system infection, head injury, epilepsy, multiple sclerosis, toxic metabolic diseases, intracranial tumors, hypothyroidism, diabetes and other physical diseases; ?Schizophrenia History of mental illness, manic episode, bipolar disorder, personality change, etc.; ?Have history of alcohol/drug dependence or taking related drugs to improve cognition; ?Combined with serious heart, liver, kidney, brain and hematopoietic diseases; ?Electronics It is contraindicated with MRI scans such as metal device implantation; ?Have a history of electric convulsions; ?T2-weighted MRI shows cerebral infarction or vascular injury; ?Allergy to edaravone dexkanol.

Design outcomes

Primary

MeasureTime frame
UNIFIED PARKINSON'S DISEASE RATING SCALE;Hamilton Depression Scale;

Secondary

MeasureTime frame
Clinical Global Impression Improvement, CGI-I;PD questionnaire 39 dimensions,PDQ-39;Hamilton Anxiey Scale;Montreal Cognitive Assessment;Mini-Mental State Examination;Parkinson's disease non-motor symptom scale;Blood inflammatory mediators;Functional magnetic resonance imaging data;Magnetoencephalogram data;electroencephalogram data;

Countries

China

Contacts

Public ContactWeiguo Liu
liuweiguo1111@sina.com13914725569

Outcome results

None listed

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