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Bradycardia clinical trials

View clinical trials related to Bradycardia.

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NCT ID: NCT01714362 Completed - Clinical trials for Bradycardia During Pulling of Eyeball

Autonomic Nervous System Activity and Oculocardiac Reflex.

Start date: October 2009
Phase:
Study type: Observational

Pulling the eyeball during ophthalmic surgery provokes decrease in heart rate. This phenomenon is called oculocardiac reflex. In some patients asystole may occur. Other cardiac features of this reflex include hypotension, dysrhythmias, atrioventricular block. These cardiovascular disturbances may lead to decreased perfusion and ischemia of vital organs. Patients with existing cardiovascular disease are in risk of complications. Cardiovascular system is mainly innervated with autonomic nervous system (ANS). Sympathetic/parasympathetic activity may be determined by Heart Rate Variability (HRV). HRV analysis based on short 5 minutes electrocardiography has been found useful for prediction of hypotension and bradycardia during induction of general anaesthesia and during spinal block. The aim of this study is to verify whether it is possible to predict oculocardiac reflex with the use of HRV analysis for ANS activity assessment, measured prior to the ophthalmic surgery.

NCT ID: NCT01700244 Active, not recruiting - Clinical trials for Normal Sinus Rhythm With 2 or 3° AV or BBB Block

Evaluation of a New Cardiac Pacemaker

Start date: December 2012
Phase: N/A
Study type: Interventional

An evaluation of a safety and performance of a new cardiac pacemaker

NCT ID: NCT01688843 Completed - Bradycardia Clinical Trials

Safety and Performance Study of the INGEVITY Lead

Start date: October 2012
Phase: N/A
Study type: Interventional

The objective of this study is to gather data to establish the safety, performance and effectiveness of the INGEVITY pace/ sense leads.

NCT ID: NCT01647490 Recruiting - Bradycardia Clinical Trials

Right Ventricular Lead Placement in a Pacemaker Population: Evaluation of Apical and Alternative Position

Start date: April 2012
Phase: N/A
Study type: Interventional

This study is a long-term, prospective, and controlled evaluation of the mechanical dyssynchrony induced by right ventricular apical pacing, both in acute (spontaneous and stimulated) and chronic (12 and 24 months); the study also evaluates the benefit of an alternative pacing site through measures of dyssynchrony in acute and chronic.

NCT ID: NCT01629186 Completed - Bradycardia Clinical Trials

Nose-close and Abdomen-compression in Pediatric Flexible Bronchoscopy

NPO-NC-AC
Start date: January 2007
Phase: N/A
Study type: Interventional

The nasopharyngeal oxygen (NPO) with Nose-close (NC) and Abdomen-compression (AC) technique may use for support or rescue asphyxiated infants during Flexible bronchoscopy.

NCT ID: NCT01595399 Recruiting - Bradycardia Clinical Trials

Atropine Versus no Atropine for Neonatal Rapid Sequence Intubation

Start date: April 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare heart rate in infants who receive atropine as a part of their medication before intubation to those who do not. To be able to find out , we need to divided babies into 2 groups; group 1 : receives atropine + sedation + muscle relaxant group 2 : receives water or saline ( placebo group) + sedation + muscle relaxant Then we need to compare heart rate during intubation and duration of intubation between the 2 groups.

NCT ID: NCT01559311 Completed - Bradycardia Clinical Trials

ENHANCE-Efficacy of the Presence of Right Ventricular Apical Pacing Induced Ventricular Dyssynchrony as a Guiding Parameter for Biventricular Pacing in Patients With Bradycardia and Normal Ejection Fraction

ENHANCE
Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of this clinical project is to evaluate the efficacy of the presence of Right Ventricular Apical (RVA) pacing induced ventricular dyssynchrony as a guiding parameter for bi-ventricular pacing in patients with bradycardia and normal left ventricular ejection fraction (LVEF). The results of this project may provide with the evidence based medicine for guidelines expansion of using Cardiac resynchronization therapy (CRT) in patients with Heart Block and normal LVEF (LVEF >45%).

NCT ID: NCT01537718 Completed - Bradycardia Clinical Trials

Evaluation of the Performances of the Sleep Disordered Breathing Monitoring Function in Pacemaker

DREAM
Start date: March 2012
Phase: Phase 3
Study type: Interventional

The IBSY04 clinical investigation is an European, prospective, multi-centre, non-randomized, longitudinal study.

NCT ID: NCT01535404 Terminated - Bradyarrhythmia Clinical Trials

Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ventricular Systolic Function Study

RIVELA
Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare chronic (1-year) effects on left ventricular ejection fraction resulting from transvenous pacing of the right ventricular apex (RVA) versus the left ventricular apex (LVA) in patients with preserved or mildly reduced left ventricular systolic function (>= 45%).

NCT ID: NCT01528150 Completed - Bradycardia Clinical Trials

Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing Indication

TendrilMRI™
Start date: February 2012
Phase:
Study type: Observational [Patient Registry]

The purpose of this observational study is the assessment (safety and efficacy) of the St. Jude Medical Tendril MRI™ leads. The Tendril MRI™ leads are a full part of the Accent MRI™ System, consisting of Tendril MRI™ leads and Accent MRI™ pacemaker. The subject population includes patients with a standard bradycardia pacing indication.