The Effect of CRT on the Frank Starling Mechanism (CRT)
Pacemaker, Heartfailure
About this trial
This is an interventional basic science trial for Pacemaker focused on measuring Frank Starling Mechanism, CRT
Eligibility Criteria
Inclusion Criteria: • Ability to provide informed consent to participate and willing to comply with the clinical investigation plan and follow-up schedule. Existing dual chamber pacemaker or ICD including atrial lead and RV lead. RV pacing percentage >40%. CRT group - Severe left ventricular systolic impairment (LVEF≤35%). Clinical symptoms of heart failure despite optimum medical therapy (NYHA class II-IV). Control group - LVEF >50%. Exclusion Criteria: • Previous treated with CRT (existing LV lead/His-Bundle lead/Left Bundle Branch Area lead). Persistent atrial fibrillation Female participants who are pregnant, lactating or planning pregnancy during the course of the study. Participation in other studies with active treatment / investigational arm
Sites / Locations
- Guy's and St Thomas' NHS Trust
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
CRT Group
Control Group
CRT group: We will include patients with symptomatic heart failure (LV ejection fraction <35% on TTE, NYHA II-IV) and an RV pacing percentage of >40%, thus meeting ESC Criteria for CRT upgrade.
Control group: patients with an existing dual chamber pacemaker and with preserved ejection fraction