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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 May 5, 2026, 7:17 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

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

  • Mirapex Drug
  • Requip Drug

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
Dec 31, 2004
Primary completion
Aug 31, 2010
Completion
Not listed
Last update posted
Mar 13, 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 13, 2014 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00144300 live on ClinicalTrials.gov.

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