Department of Cardiology - CHU Pontchaillou
Rennes, 35011, France
NCT Number: NCT00187265
The purpose of this study is to evaluate the feasibility of permanent biventricular pacing using three ventricular leads, and its efficacy in terms of inter and intra-ventricular resynchronization, in patients with congestive heart failure and a non-functional atrium (chronic AF).
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Rennes, 35011, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
The medical treatment must include a 40 mg/day minimum dose of furosemide (or equivalent);
Exclusion criteria
Abbott Medical Devices
Industry
Triple Resynchronization in Paced Heart Failure Patients
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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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