Observational Study of Pergolide Mesylate and Cardiac Valvulopathy

Lilly

Status: Completed

Conditions: Parkinson Disease

Study type: Observational

Funder types: Industry

Identifiers

NCT00311532

B4G-MC-B001

10245

Details and patient eligibility

About

The primary objective of this study is to estimate the incidence of new-onset valvulopathy, determined by baseline and follow-up echocardiograms, in patients with Parkinson's Disease who are receiving pergolide as second-line therapy.

The secondary objective of the study is to estimate the prevalence of valvulopathy, as determined by baseline echocardiograms, among all patients who have Parkinson's Disease and are being considered for pergolide as second-line therapy.

Enrollment: 200 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female, age 18 and older with a diagnosis of Parkinson's Disease
• Receiving pergolide as second-line therapy as prescribed by Summary of Product Characteristics
• Willing to participate and sign a consent to release medical information
• Have had an echocardiogram within 3 months of initiation of pergolide therapy with no evidence of cardiac valvulopathy

Exclusion criteria

• There are no exclusion criteria for this study