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Pergolide Treatment and Valvular Heart Disease
This study has been completed.
Sponsored by: Århus Amt
Information provided by: Århus Amt
ClinicalTrials.gov Identifier: NCT00234364
  Purpose

In a blinded echocardiographic study we investigate the frequency of valvular abnormalities in a group of Parkinson patients treated with either ergot derived dopamine agonists (pergolide and cabergoline) or non-ergot derived dopamine agonists (pramipexole and ropinirole). The ability to detect patients with valvular abnormalities by clinical approach is examined.


Condition
Heart Valve Diseases
Parkinson's Disease
Pergolide
Fibrosis

Genetics Home Reference related topics: familial paroxysmal nonkinesigenic dyskinesia Parkinson disease
MedlinePlus related topics: Heart Diseases Heart Valve Diseases Parkinson's Disease
Drug Information available for: Pergolide Pergolide mesylate Ergotamine Ergotamine tartrate
U.S. FDA Resources
Study Type: Observational
Study Design: Screening, Cross-Sectional, Defined Population, Retrospective/Prospective Study

Further study details as provided by Århus Amt:

Enrollment: 155
Study Start Date: March 2005
Study Completion Date: September 2007
Detailed Description:

Some case reports and a single study, which included 78 Parkinson patients, has found a correlation between treatment with the ergotamine derivative dopamine agonists (pergolide) and restrictive valvular heart disease. The mechanisms are thought to be the same as with the former used anorectikum, fenfluramine and other drugs stimulating the 5HT-2B receptor.

In a blinded manner we make physiologic and echocardiographic examination on 160 Parkinson patients treated with either ergotamine or non-ergotamine derivative dopamine agonists (80 patients in each group) to see whether Parkinson patients treated with ergotamine derivatives have more heart valvular disease

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Parkinson patients who in the last year has been treated minimum 6 months with either ergotamine derivative or non-ergotamine derivative dopamine agonists (the latter included as controls)
  • Informed contests

Exclusion Criteria:

  • Control patients will be excluded if the have been treated with ergotamine derivates in the last 12 months or if the prior to that have had ergotamine derivates for more than 6 months
  • Patients with known valvular heart disease prior to the diagnosis of Parkinson
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00234364

Locations
Denmark, Aahus N
Skejby Hospital
Aarhus, Aahus N, Denmark, 8200
Sponsors and Collaborators
Århus Amt
Investigators
Principal Investigator: Vibeke G Rasmussen, MD Skejby Hospital
  More Information

Study ID Numbers: permax
Study First Received: October 4, 2005
Last Updated: September 19, 2007
ClinicalTrials.gov Identifier: NCT00234364  
Health Authority: Denmark: The Regional Committee on Biomedical Research Ethics

Keywords provided by Århus Amt:
Pergolide
Ergotamine derivates
Valvular heart disease

Study placed in the following topic categories:
Heart Diseases
Ganglion Cysts
Fibrosis
Basal Ganglia Diseases
Central Nervous System Diseases
Ergotamine
Brain Diseases
Neurodegenerative Diseases
Heart Valve Diseases
Parkinson Disease
Movement Disorders
Parkinsonian Disorders
Pergolide

Additional relevant MeSH terms:
Pathologic Processes
Nervous System Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009