Erfurt, Thuringia, 99084, Germany
NCT Number: NCT00568945
Study to Investigate the Effect of the A1 Agonist Capadenoson on Ventricular HR in Patients With Persistent or Permanent Atrial Fibrillation.
This trial has the primary goal to show that BAY68-4986 can lower the ventricular rate in patients with the indication persistent atrial fibrillation.
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Notify MeKey information
Conditions
Age range
18 year–75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Male and/or female (without childbearing potential) white patients
- History of persistent or permanent atrial fibrillation
- 18 to 75 years of age
Exclusion criteria
- Patients with high-risk cardiovascular diseases
- Stroke or myocardial infarction
- Relevant pathological changes in the ECG or echocardiography
- Medication affecting ventricular response in Afib
Treatment and study plan
Capadenoson (BAY68-4986)
Drug4 mg BAY68-4986 for five days
Primary outcomes
-
The effect of capadenoson (BAY68-4986) on rate control in patients with atrial fibrillation
Time frame: 1 week
Secondary outcomes
-
To investigate safety and tolerability of this treatment with capadenoson
Time frame: 2 weeks
Sponsors and collaborators
Lead sponsor
Bayer
Industry
Registry information
Official study title
Study to Investigate the Effect of the A1 Agonist Capadenoson on Ventricular HR in Patients With Persistent or Permanent Atrial Fibrillation by Administration of Capadenoson in a Dose of 4 mg Once Daily for Five Days
Important dates
- Study start
- 2008
- Primary completion
- 2008
- Study completion
- 2008
- First posted
- Dec 6, 2007
- Registry last updated
- Oct 29, 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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