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Completed Phase 4 Interventional Results available

Study of (Mirapex) Pramipexole for the Early Treatment of Parkinsons Disease (PD)

ClinicalTrials.gov ID: NCT00321854

Public ClinicalTrials.gov record NCT00321854. 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 Sep 28, 2026, 5:53 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 Randomized, Double-blind, Placebo-controlled, Parallel-group Clinical Trial to Examine the Efficacy and Safety of Early Pramipexole (PPX) Treatment Versus Delayed Pramipexole Treatment in Patients With New Onset Parkinson's Disease.

Brief summary

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

This is a double blind, placebo-controlled clinical trial of 15 months duration designed to examine early Mirapex (pramipexole) treatment vs. delayed Mirapex (pramipexole) treatment in patients with new onset Parkinsons disease

Study identification

NCT ID
NCT00321854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
535 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
30 Years to 79 Years
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
Apr 30, 2006
Primary completion
Mar 31, 2009
Completion
Not listed
Last update posted
May 15, 2014

Started 2006

United States locations

U.S. sites
32
U.S. states
19
U.S. cities
31
Facility City State ZIP Site status
248.595.0122 Boehringer Ingelheim Investigational Site Brimingham Alabama — —
248.595.0104 Boehringer Ingelheim Investigational Site Scottsdale Arizona — —
248.595.0133 Boehringer Ingelheim Investigational Site La Jolla California — —
248.595.0140 Boehringer Ingelheim Investigational Site La Jolla California — —
248.595.0112 Boehringer Ingelheim Investigational Site New Haven Connecticut — —
248.595.0113 Boehringer Ingelheim Investigational Site Bradenton Florida — —
248.595.0105 Boehringer Ingelheim Investigational Site Gainesville Florida — —
248.595.0119 Boehringer Ingelheim Investigational Site Hollywood Florida — —
248.595.0124 Boehringer Ingelheim Investigational Site Palm Beach Gardens Florida — —
248.595.0123 Boehringer Ingelheim Investigational Site Panama City Florida — —
248.595.0109 Boehringer Ingelheim Investigational Site South Miami Florida — —
248.595.0115 Boehringer Ingelheim Investigational Site St. Petersburg Florida — —
248.595.0106 Boehringer Ingelheim Investigational Site Tampa Florida — —
248.595.0103 Boehringer Ingelheim Investigational Site Atlanta Georgia — —
248.595.0127 Boehringer Ingelheim Investigational Site Augusta Georgia — —
248.595.0137 Boehringer Ingelheim Investigational Site Columbus Georgia — —
248.595.0101 Boehringer Ingelheim Investigational Site Chicago Illinois — —
248.595.0111 Boehringer Ingelheim Investigational Site Elk Grove Village Illinois — —
248.595.0131 Boehringer Ingelheim Investigational Site Scarbourough Maine — —
248.595.0134 Boehringer Ingelheim Investigational Site Baltimore Maryland — —
248.595.0141 Boehringer Ingelheim Investigational Site Worcester Massachusetts — —
248.595.0102 Boehringer Ingelheim Investigational Site Traverse City Michigan — —
248.595.0129 Boehringer Ingelheim Investigational Site New York New York — —
248.595.0139 Boehringer Ingelheim Investigational Site Raleigh North Carolina — —
248.595.0136 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina — —
248.595.0120 Boehringer Ingelheim Investigational Site Cleveland Ohio — —
248.595.0107 Boehringer Ingelheim Investigational Site Dayton Ohio — —
248.595.0118 Boehringer Ingelheim Investigational Site Tulsa Oklahoma — —
248.595.0114 Boehringer Ingelheim Investigational Site Warwick Rhode Island — —
248.595.0116 Boehringer Ingelheim Investigational Site Memphis Tennessee — —
248.595.0108 Boehringer Ingelheim Investigational Site Houston Texas — —
248.595.0121 Boehringer Ingelheim Investigational Site Kirkland Washington — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 67 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00321854, 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 May 15, 2014 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00321854 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →