NCT Number: NCT02236741
The Use of Pramipexole and Other Dopamine Agonists and the Risks of Heart Failure and Pneumonia
Study to assess the risk of incident heart failure associated with the use of pramipexole compared with other dopamine agonists and additionally, to assess the risk of incident heart failure associated with the use of dopamine agonists in comparison with no use of dopamine agonist therapy
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Notify MeKey information
Conditions
Age range
40 year–89 year
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- All patients between 40 and 89 years of age who received at least one prescription for anti-parkinsonian drugs during the period 1997-2009
Exclusion criteria
- Patients with a diagnosis of heart failure or with prescriptions for two or more among the digitalis, angiotensin-converting enzyme (ACE) inhibitors/angiotensin receptor blocker (ARB), and diuretic drug classes prior to cohort entry
Treatment and study plan
Primary outcomes
-
Assessment of first-time clinical diagnosis of heart failure
Time frame: 150 months
Secondary outcomes
-
Overall rate of heart failure
Time frame: 150 months
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Important dates
- Study start
- 2009
- Primary completion
- 2010
- First posted
- Sep 11, 2014
- Registry last updated
- Sep 11, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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