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Pharmacology of levodopa/carbidopa versus levodopa/benserazide in patients with parkinson's disease

Pharmacology of levodopa/carbidopa versus levodopa/benserazide in patients with parkinson's disease

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039201
Enrollment
Unknown
Registered
2020-10-21
Start date
2020-11-15
Completion date
Unknown
Last updated
2021-01-18

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

Conditions

Parkinson's disease

Interventions

A:phase I: levodopa/carbidopa
phase II: levodopa/benserazide
B:phase I: levodopa/benserazide
phase II: levodopa/carbidopa

Sponsors

The Affiliated Brain Hospital of Nanjing Medical University (Nanjing Brain Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Primary PD patients (diagnosed according to the 2015 MDS diagnostic criteria); 2. Long-term use of anti-PD drugs; 3. Hoehn and Yahr [H&Y] stage > or = 3; 4. Men and women with aged 30-85 years;5.Inform consent form.

Exclusion criteria

Exclusion criteria: 1. Hoehn and Yahr [H&Y] stage < 3; 2. Serious impairment of liver, kidney, heart and lung function; 3. Severe anemia; 4. Deep brain stimulation history; 5. Disease that is considered to interfere with research (Such as diarrhea and/or gastrointestinal malabsorption); 6. Allergic to any of the experimental drugs; 7. Demented PD; Pregnant woman; 8. Women who are pregnant or breastfeeding; 9. Alcohol or drug dependence; 10. Patients are participating in other clinical studies or have participated in other clinical studies in the previous 30 days.

Design outcomes

Primary

MeasureTime frame
Levodopa plasma concentration;Carbidopa plasma concentration;Benserazide plasma concentration;MDS-UPDRS III;Dopamine plasma concentration;

Countries

China

Contacts

Public ContactWeiguo Liu

The Fourth Affiliated Hospital of Nanjing Medical University

wgliunbh@sina.com+86 13914725569

Outcome results

None listed

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