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Atrioventricular Block clinical trials

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NCT ID: NCT01922518 Completed - Clinical trials for Atrioventricular Block

Impact of Right Ventricular Pacing Determined by Electrocardiography

RVpacing
Start date: March 2013
Phase: N/A
Study type: Interventional

Typically pacemaker electrode has been attached to the right ventricular apex. This method lead to Non-physiological Ventricular contraction. It has been reported to cause by ventricular dysfunction. In conclusion, this study demonstrate that impact of right ventricular pacing determined by electrocardiography was planned.

NCT ID: NCT01019213 Completed - Clinical trials for Atrioventricular Block

Acute and Chronic Effect of His-pacing in Consecutive Patients With AV-block

Start date: September 2007
Phase: Phase 4
Study type: Interventional

Conventional right ventricular (RV) apical pacing may result in asynchronous ventricular contraction with delayed left ventricular activation, interventricular motion abnormalities, and worsening of left ventricular ejection fraction. His pacing is preserving a synchronous contraction and may prevent a decrease in left ventricular ejection fraction. Hypothesis: His-pacing preserves left ventricular function and is a feasable alternative compared to RV septal septal pacing in patients with AV-block.

NCT ID: NCT00925691 Completed - Clinical trials for Atrioventricular Block

Comparison of SEPTal and Apical Pacing Sites in PerManent Right Ventricular Pacing

SEPTAL-PM
Start date: April 2010
Phase: Phase 3
Study type: Interventional

The SEPTAL-PM study is aimed to compare the right ventricular apical and right ventricular septal position of the right ventricular lead in patients implanted with a pacemaker for conventional anti-bradycardia pacing indications requiring permanent right ventricular pacing ; the primary endpoint is the evolution of the left ventricular ejection fraction assessed by contrast echocardiography at 18-months follow-up.

NCT ID: NCT00832260 Completed - Sinus Node Disease Clinical Trials

IES-ACap: Influence of Atrial Pulse Width in the Behaviour of ACap™ Confirm Algorithm.

IES-ACap
Start date: January 2009
Phase:
Study type: Observational

The purpose of this observational study is to collect data regarding the population of patients with a pacemaker implanted.

NCT ID: NCT00655213 Completed - Clinical trials for Sinus Node Dysfunction

Spontaneous Atrio Ventricular Conduction Preservation

SAVER
Start date: November 2003
Phase: Phase 4
Study type: Interventional

In case of sinus node dysfunction, it is often necessary to choose the safer option provided by a DDD pacemaker even though the most appropriate mode of pacing is AAI mode. In addition to saving energy, the latter mode allows spontaneous ventricular activation, the haemodynamic consequences of which are, in most cases, better than those obtained with dual chamber pacing. Recent studies as the MOST study suggest also that ventricular desynchronization imposed by right ventricular apical pacing even when AV synchrony is preserved increases the risk of atrial fibrillation in patients with SND. Similar results were already given by anterior studies (PIPAF) which, taking into account the percentage of ventricular pacing, suggested that AF prevention algorithm in combination with a preserved native conduction are efficient in reducing AF burden. However, current practice is to implant a dual chamber pacemaker to prevent the risk of atrioventricular block (AVB) even if DDDR pacing with a fixed long AV delay was found inefficient in reducing ventricular pacing and was associated with a high risk of arrhythmias. The Symphony 2550 cardiac pacemaker offers pacing modes that automatically switch from AAI(R) mode to DDD(R) or DDI(R) in event of severe atrioventricular conduction disorder, irrespective of whether or not these are accompanied by an atrial arrhythmia, returning spontaneously to AAI(R) mode as soon as the spontaneous AV conduction has resumed. These 2 particular modes are called the AAI SafeR and DDD/AMC (R) mode. The main differences between both modes are that (i) AAI SafeR does not trigger any AV Delay after a sensed or paced atrial event which allows long PR intervals or even limited ventricular pauses with no switch to DDD(R), while (ii) DDD/AMC (R) is able to optimize AV Delay after switching to DDD(R) according to measured spontaneous conduction times and to provide an acceleration in case of vaso-vagal syndrome. This pacing mode has previously been assessed in clinical studies. This study intends to demonstrate that the automatic modes switching significantly reduce the percentage of ventricular pacing in patients implanted with a spontaneous AV conduction and reduce the occurrence of atrial arrhythmias, on a mid-term follow-up period, in comparison to standard DDD pacing with long AVDelay.

NCT ID: NCT00627328 Completed - Atrial Fibrillation Clinical Trials

The Atrial High Rate Episodes in Pacemaker Patients

Start date: July 2000
Phase: N/A
Study type: Observational

Prospective study assessing the incidence of atrial high rate episodes (AHRE) in pacemaker patients with and without previously diagnosed AT.

NCT ID: NCT00267098 Completed - Heart Diseases Clinical Trials

Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With Atrioventricular Block (BLOCK HF)

BLOCK HF
Start date: December 2003
Phase: N/A
Study type: Interventional

Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. When there are changes in the heartbeat, sometimes a pacemaker is used to control the rate and rhythm of the heartbeat. In this trial, the researchers will test if pacing both the left and right lower half of the heart (ventricles) will: - decrease the number of hospital and clinic visits due to heart failure symptoms - extend life - delay heart failure symptoms as compared to those who are paced in only one ventricle (the right ventricle)

NCT ID: NCT00187278 Completed - Clinical trials for Ventricular Dysfunction

Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardiac Desynchronization

Start date: May 2003
Phase: N/A
Study type: Interventional

The primary purpose of the study is to evaluate if patients with a standard indication for permanent ventricular pacing, left ventricular ejection fraction without limit, or any QRS duration will profit from the prevention of ventricular desynchronisation.