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Completed Phase 4 Interventional Results available

A Randomized, Double-blind, Active (Pramipexole 0.5 mg Tid) and Placebo Controlled, Study of Pramipexole Given 0.5 mg and 0.75 mg Bid Over 12-week Treatment in Early Parkinson's Disease (PD) Patients

ClinicalTrials.gov ID: NCT00402233

Public ClinicalTrials.gov record NCT00402233. 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 3, 2026, 4:46 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, Active (Pramipexole 0.5 mg Tid) and Placebo Controlled, Efficacy Study of Pramipexole Given 0.5 mg and 0.75 mg Bid Over a 12-week Treatment Phase in Early Parkinson's Disease Patients (PramiBID)

Brief summary

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

Primary objective: to assess the efficacy of pramipexole given two times daily compared to placebo. Secondary objectives: to assess the effects of pramipexole on mood, cognition, fatigue, impulse control, daytime sleepiness and nighttime sleep compared to placebo; to compare the tolerability among the treatment groups over 12 weeks

Study identification

NCT ID
NCT00402233
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
312 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
31 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
Oct 31, 2006
Primary completion
Aug 31, 2008
Completion
Not listed
Last update posted
May 15, 2014

Started 2006

United States locations

U.S. sites
39
U.S. states
20
U.S. cities
35
Facility City State ZIP Site status
248.622.170 Boehringer Ingelheim Investigational Site Phoenix Arizona
248.622.112 Boehringer Ingelheim Investigational Site Little Rock Arkansas
248.622.69 Boehringer Ingelheim Investigational Site Fountain Valley California
248.622.198 Boehringer Ingelheim Investigational Site La Jolla California
248.622.111 Boehringer Ingelheim Investigational Site Oxnard California
248.622.61 Boehringer Ingelheim Investigational Site Sacramento California
248.622.23 Boehringer Ingelheim Investigational Site San Diego California
248.622.73 Boehringer Ingelheim Investigational Site San Francisco California
248.622.108 Boehringer Ingelheim Investigational Site Denver Colorado
248.622.190 Boehringer Ingelheim Investigational Site Danbury Connecticut
248.622.215 Boehringer Ingelheim Investigational Site Manchester Connecticut
248.622.196 Boehringer Ingelheim Investigational Site Boca Raton Florida
248.622.14 Boehringer Ingelheim Investigational Site Miami Florida
248.622.149 Boehringer Ingelheim Investigational Site Weston Florida
248.622.139 Boehringer Ingelheim Investigational Site Honolulu Hawaii
248.622.5 Boehringer Ingelheim Investigational Site Chicago Illinois
248.622.138 Boehringer Ingelheim Investigational Site Springfield Illinois
248.622.87 Boehringer Ingelheim Investigational Site Louisville Kentucky
248.622.207 Boehringer Ingelheim Investigational Site New Orleans Louisiana
248.622.132 Boehringer Ingelheim Investigational Site Shreveport Louisiana
248.622.17 Boehringer Ingelheim Investigational Site Boston Massachusetts
248.622.40 Boehringer Ingelheim Investigational Site Boston Massachusetts
248.622.76 Boehringer Ingelheim Investigational Site Boston Massachusetts
248.622.186 Boehringer Ingelheim Investigational Site East Lansing Michigan
248.622.77 Boehringer Ingelheim Investigational Site Omaha Nebraska
248.622.155 Boehringer Ingelheim Investigational Site Lebanon New Hampshire
248.622.135 Boehringer Ingelheim Investigational Site Brooklyn New York
248.622.216 Boehringer Ingelheim Investigational Site Kingston New York
248.622.202 Boehringer Ingelheim Investigational Site New York New York
248.622.86 Boehringer Ingelheim Investigational Site New York New York
248.622.1 Boehringer Ingelheim Investigational Site Rochester New York
248.622.89 Boehringer Ingelheim Investigational Site Cincinnati Ohio
248.622.20 Boehringer Ingelheim Investigational Site Columbus Ohio
248.622.169 Boehringer Ingelheim Investigational Site Hershey Pennsylvania
248.622.18 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
248.622.199 Boehringer Ingelheim Investigational Site Houston Texas
248.622.7 Boehringer Ingelheim Investigational Site Houston Texas
248.622.213 Boehringer Ingelheim Investigational Site Spokane Washington
248.622.104 Boehringer Ingelheim Investigational Site Milwaukee Wisconsin

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 NCT00402233, 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 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00402233 live on ClinicalTrials.gov.

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