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The Effect of Sifrol® on Tremor and Depression in Patients With Idiopathic Parkinson's Disease

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Parkinson Disease

Treatments

Drug: Sifrol®

Study type

Observational

Funder types

Industry

Identifiers

NCT02231294
248.511

Details and patient eligibility

About

Documentation of the effect of SIFROL® on tremor and depression as well as its tolerability in ambulatory patients suffering from idiopathic Parkinson's disease under routine conditions

Enrollment

1,464 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with idiopathic Parkinson's disease with tremor and/or depression requiring therapy with Sifrol® or change of therapy to Sifro®l and not under medication with neuroleptics were allowed to be observed during the study

Exclusion criteria

  • Patients who meet one or more of the general or specific contraindications mentioned in the Summary of Product Characteristics (SPC) for Sifrol®
  • Patients under treatment with neuroleptics should not be observed during this study

Trial design

1,464 participants in 1 patient group

Idiopathic Parkinson's Disease Patients
Treatment:
Drug: Sifrol®

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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