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Cardiac Pacing, Artificial clinical trials

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NCT ID: NCT04505384 Completed - Heart Failure Clinical Trials

Acute Effects of LBBP Versus BVP for CRT

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The study was designed to compare the acute effects of left bundle branch pacing (LBBP) with biventricular pacing (BVP) in patients with left ventricular ejection fraction (LVEF) <=35% with left bundle branch block (LBBB).

NCT ID: NCT03452462 Completed - Clinical trials for Cardiac Resynchronization Therapy

Electrical Resynchronization and Acute Hemodynamic Effects of Direct His Bundle Pacing Compared to Biventricular Pacing

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The aims are to compare Direct His Bundle Pacing (DHBP) with biventricular pacing (BiV) in terms of electrical resynchronization using electrocardiographic imaging (ECGI) and also in terms of acute hemodynamical effect using finger plethysmography and conduction velocimetry. The study will be a randomized crossover design with acute measurements.

NCT ID: NCT03388281 Completed - Clinical trials for Cardiac Pacing, Artificial

Morbidity, Mortality and Gender Differences in Patients With Pacemakers

Start date: July 28, 2015
Phase: N/A
Study type: Observational

Previous publications suggest gender difference in outcome parameters after pacemaker implantation. Aim of this study is to investigate gender differences in patients with pacemaker. Implanted devices, indication for implantation and pacemaker follow up data of patients will be included. Survival data including cause of death will be documented. Prevalent comorbidities and relevant laboratory data will be recorded.

NCT ID: NCT03281395 Completed - Aneurysm, Brain Clinical Trials

Rapid Ventricular Pacing During Cerebral Aneurysm Surgery: a Retrospective Study Concerning the Safety for Heart and Brain

Start date: August 30, 2011
Phase: N/A
Study type: Observational

Rapid ventricular pacing (RVP) is a technique to obtain flow arrest for short periods of time during dissection or rupture of the aneurysm. RVP results in an adequate fall of blood pressure which presents as an on-off phenomenon. It is not clear whether repetitive periods of pacing are harmless for the patient. Silent cardiac and cerebral infarcts may be undetected. The investigator will study the safety of RVP, particularly for the heart and the brain, retrograde by studying troponin levels and magnetic resonance imaging or computed tomography.

NCT ID: NCT00541541 Completed - Clinical trials for Heart Failure, Congestive

Acoustic Cardiographic Assessment of Heart Function and the Role of Phrenic Nerve Stimulation

Start date: February 2007
Phase: N/A
Study type: Interventional

In this study, the investigators sought to determine whether a stimulation of the phrenic nerve affects heart function. Heart function is assessed by acoustic cardiography.

NCT ID: NCT00417092 Completed - Clinical trials for Coronary Artery Bypass

Biventricular Pacing After Coronary Artery Bypass Grafting (BIVAC)

Start date: December 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine which pacing mode after coronary artery bypass grafting in patients with reduced left ventricular function is hemodynamically favorable.

NCT ID: NCT00399594 Completed - Clinical trials for Heart Failure, Congestive

Effect of Targeting Left Ventricular Lead Position on the Rate of Response to Cardiac Resynchronization Therapy.

INCREMENTAL
Start date: March 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Identifying & optimizing strategies to reduce the burden of heart failure is vital. Despite advances in pharmacotherapy, patients with heart failure are at high risk for death & hospitalization. Cardiac resynchronization therapy (CRT) synchronizes ventricular mechanical activity, improves cardiac output & reduces HF symptoms. However, ~50% of patients do not clearly respond to CRT. Sub-optimal placement of the LV pacing lead appears to be an important reason for non-response. This study will assess whether targeted LV lead placement will result in an increased probability of CRT response at 52 weeks vs. usual (lateral wall) lead placement.

NCT ID: NCT00323661 Completed - Clinical trials for Cardiac Pacing, Artificial

Closed Loop Stimulation, Cognitive Performance, and Quality of Life in Pacemaker Patients

COGNITION
Start date: May 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the influence of accelerometer-based rate adaptation and Closed Loop Stimulation on cognitive performance and quality of life in pacemaker patients.