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Completed Phase 4 Interventional Results available

Ophthalmologic Safety Study of Pramipexole Immediate Release (IR) Versus Ropinirole in Early Parkinson's Disease (PD) Patients

ClinicalTrials.gov ID: NCT00144300

Public ClinicalTrials.gov record NCT00144300. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 5:15 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Two Year Open Label, Randomized, Parallel Group, Blinded Assessment Ophthalmologic Safety Study of Pramipexole IR Versus Ropinirole in Early Parkinson's Disease Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To determine if there is any difference in the presence of retinal deterioration in PD patients treated with pramipexole IR versus ropinirole as monitored by comprehensive ophthalmologic assessments from baseline to the end of study at two years.

Study identification

NCT ID
NCT00144300
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
246 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
30 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2005 (Type not available)
Primary completion
Sep 2010 (Actual)
Completion
Not listed
Last update posted
Mar 14, 2014

Started 2005

United States locations

U.S. sites
21
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
248.538.00007 Boehringer Ingelheim Investigational Site Birmingham Alabama — —
248.538.00008 Boehringer Ingelheim Investigational Site Little Rock Arkansas — —
248.538.00021 Boehringer Ingelheim Investigational Site Fountain Valley California — —
248.538.00022 Boehringer Ingelheim Investigational Site Los Angeles California — —
248.538.00001 Boehringer Ingelheim Investigational Site New Haven Connecticut — —
248.538.00002 Boehringer Ingelheim Investigational Site Miami Florida — —
248.538.00016 Boehringer Ingelheim Investigational Site Tampa Florida — —
248.538.00023 Boehringer Ingelheim Investigational Site Tampa Florida — —
248.538.00013 Boehringer Ingelheim Investigational Site Atlanta Georgia — —
248.538.00009 Boehringer Ingelheim Investigational Site Augusta Georgia — —
248.538.00011 Boehringer Ingelheim Investigational Site Chicago Illinois — —
248.538.00005 Boehringer Ingelheim Investigational Site Baltimore Maryland — —
248.538.00014 Boehringer Ingelheim Investigational Site Southfield Michigan — —
248.538.00010 Boehringer Ingelheim Investigational Site New York New York — —
248.538.00015 Boehringer Ingelheim Investigational Site New York New York — —
248.538.00020 Boehringer Ingelheim Investigational Site New York New York — —
248.538.00012 Boehringer Ingelheim Investigational Site Charlotte North Carolina — —
248.538.00006 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania — —
248.538.00004 Boehringer Ingelheim Investigational Site Memphis Tennessee — —
248.538.00003 Boehringer Ingelheim Investigational Site Houston Texas — —
248.538.00017 Boehringer Ingelheim Investigational Site Morgantown West Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00144300, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 14, 2014 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00144300 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →