About this study
RESTORE-HF is a planned study of the UPright™ System. It is waiting for approval from the US Food and Drug Administration (FDA) and has not started. Procedures are planned at hospitals in the United States and Europe.
Randomizedparticipants are randomly assigned to receive either the device or a similar procedure without it
Double-blindparticipants and the doctors who assess them are not told whether the implants were placed
Who can take part, and where, will be published after FDA approval. Your study doctor will explain the procedure, the follow-up visits, and the possible risks and benefits before you decide.
Always talk to your own doctor about your condition and treatment options.