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Efficacy of entacapone and pramipexole for non-motor symptoms of Parkinson’s disease: a prospective randomized controlled trial

Efficacy of entacapone and pramipexole for non-motor symptoms of Parkinson’s disease: a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022534
Enrollment
Unknown
Registered
2019-04-15
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

non-motor symptoms of Parkinson’s disease

Interventions

entacapone group:Patients in the entacapone group will be administered entacapone (Novartis
import drug registration certificate number: H20160680), 10 times per day, 200 mg each time, for 3 weeks.
pramipexole group:Patients in the pramipexole group will be administered pramipexole (Boehringer-Ingelheim
import drug registration certificate number: 20140918) , 3 times per day, 1 mg each time, for 3 weeks.

Sponsors

Geriatric Hospital of Hainan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1 Accordance with British Brain Bank Diagnostic Criteria for idiopathic Parkinson's Disease; 2 Record daily activities correctly; 3 Patient age 40 to 75 years, irrespective of sex; 4 Provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1 History of drug abuse; 2 Schizophrenia or severe cognitive impairment; 3 Epilepsy; 4 Severe metabolic dysfunction such as diabetes mellitus; 5 Malignant tumor; 6 Participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Improvement rate of non-motor symptoms;

Secondary

MeasureTime frame
Serum soluble interleukin-2 receptor levels;Serum homocysteine levels;Adverse events;

Countries

China

Contacts

Public ContactZheng Bei

Geriatric Hospital of Hainan

zmjidf@163.com+86 13876908681

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026