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Terminated Phase 2 Interventional Results available

Pramipexole ER vs. Placebo in Fibromyalgia

ClinicalTrials.gov ID: NCT00689052

Public ClinicalTrials.gov record NCT00689052. 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 Jul 21, 2026, 1:45 PM 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, Dose Titration Efficacy and Safety Study of Pramipexole ER (0.75 to 4.5 mg) Administered Orally Once Daily Versus Placebo Over a 16-week Maintenance Phase in Patients Diagnosed With Fibromyalgia, as Assessed by the American College of Rheumatology (ACR) Criteria Followed by a 24-week Open-label Extension Phase

Study identification

NCT ID
NCT00689052
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
61 participants

Conditions and interventions

Conditions

Interventions

  • pramipexole ER Drug
  • placebo Drug

Drug

Eligibility (public fields only)

Age range
18 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
Jun 30, 2008
Primary completion
Oct 31, 2008
Completion
Not listed
Last update posted
Jun 8, 2014

Started 2008

United States locations

U.S. sites
42
U.S. states
27
U.S. cities
42
Facility City State ZIP Site status
248.637.01009 Boehringer Ingelheim Investigational Site Birmingham Alabama
248.637.01033 Boehringer Ingelheim Investigational Site Phoenix Arizona
248.637.01045 Boehringer Ingelheim Investigational Site Tucson Arizona
248.637.01034 Boehringer Ingelheim Investigational Site Hot Springs Arkansas
248.637.01032 Boehringer Ingelheim Investigational Site Arcadia California
248.637.01044 Boehringer Ingelheim Investigational Site Los Angeles California
248.637.01036 Boehringer Ingelheim Investigational Site Santa Ana California
248.637.01042 Boehringer Ingelheim Investigational Site Englewood Colorado
248.637.01031 Boehringer Ingelheim Investigational Site Danbury Connecticut
248.637.01035 Boehringer Ingelheim Investigational Site DeLand Florida
248.637.01023 Boehringer Ingelheim Investigational Site Fort Myers Florida
248.637.01047 Boehringer Ingelheim Investigational Site Orlando Florida
248.637.01043 Boehringer Ingelheim Investigational Site Palm Beach Gardens Florida
248.637.01040 Boehringer Ingelheim Investigational Site Sunrise Florida
248.637.01027 Boehringer Ingelheim Investigational Site Tampa Florida
248.637.01007 Boehringer Ingelheim Investigational Site Atlanta Georgia
248.637.01028 Boehringer Ingelheim Investigational Site Chicago Illinois
248.637.01010 Boehringer Ingelheim Investigational Site Lexington Kentucky
248.637.01016 Boehringer Ingelheim Investigational Site Newton Massachusetts
248.637.01014 Boehringer Ingelheim Investigational Site Lansing Michigan
248.637.01020 Boehringer Ingelheim Investigational Site Flowood Mississippi
248.637.01018 Boehringer Ingelheim Investigational Site Picayune Mississippi
248.637.01012 Boehringer Ingelheim Investigational Site Kansas City Missouri
248.637.01017 Boehringer Ingelheim Investigational Site Billings Montana
248.637.01024 Boehringer Ingelheim Investigational Site Albuquerque New Mexico
248.637.01008 Boehringer Ingelheim Investigational Site Albany New York
248.637.01002 Boehringer Ingelheim Investigational Site New York New York
248.637.01025 Boehringer Ingelheim Investigational Site Charlotte North Carolina
248.637.01026 Boehringer Ingelheim Investigational Site Fargo North Dakota
248.637.01004 Boehringer Ingelheim Investigational Site Cincinnati Ohio
248.637.01038 Boehringer Ingelheim Investigational Site Columbus Ohio
248.637.01003 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
248.637.01046 Boehringer Ingelheim Investigational Site Medford Oregon
248.637.01006 Boehringer Ingelheim Investigational Site Portland Oregon
248.637.01039 Boehringer Ingelheim Investigational Site Duncansville Pennsylvania
248.637.01015 Boehringer Ingelheim Investigational Site Warwick Rhode Island
248.637.01019 Boehringer Ingelheim Investigational Site Austin Texas
248.637.01037 Boehringer Ingelheim Investigational Site San Antonio Texas
248.637.01041 Boehringer Ingelheim Investigational Site Salt Lake City Utah
248.637.01021 Boehringer Ingelheim Investigational Site Renton Washington
248.637.01029 Boehringer Ingelheim Investigational Site Seattle Washington
248.637.01011 Boehringer Ingelheim Investigational Site Spokane Washington

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 NCT00689052, 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 Jun 8, 2014 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00689052 live on ClinicalTrials.gov.

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