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Bradycardia clinical trials

View clinical trials related to Bradycardia.

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NCT ID: NCT03037333 Recruiting - Bradycardia Clinical Trials

Analysis in the EMERGEncy Between TransVenous Cardiac PACIng Guided by Fluoroscopy Versus Echocardiogram

EMERG-TV-PAC
Start date: August 16, 2017
Phase: N/A
Study type: Interventional

A lot of questions about use of temporary transvenous pacing still remain obscure and there is no effective comparison between use of fluoroscopy versus electrocardiogram/echocardiogram in patients with bradicardias. The aim of the study is to evaluate how long does it take to start the correct cardiac stimulation with transvenous pacing in patients with bradicardias comparing use of fluoroscopy versus electrocardiogram/echocardiogram and compare rates of complications between two methods.

NCT ID: NCT03008291 Recruiting - Heart Failure Clinical Trials

His Bundle Pacing in Bradycardia and Heart Failure

Start date: October 2016
Phase:
Study type: Observational

Participants in this study will either have heart failure (HF) and are scheduled to undergo pace maker (PM) implantation, cardiac resynchronization therapy pacemaker (CRT-P), cardiac resynchronization therapy defibrillator (CRT-D) implantation, His bundle pacing (HIBP) or left bundle area pacing (LBAP) (including HIBP/LBAP for patients with HF, for patients who have failed CRT implant or patients who are CRT non-responders), or have atrioventricular (AV) block or bradycardia and are scheduled to undergo dual chamber pacemaker implantation. In this study additional heart rhythm measurements will be collected during the implant procedure to better understand how His bundle and/or parahisian pacing (HISP) effects electrical conduction in the hearts of patients with HF or AV block. The hypothesis is that His bundle or parahisian pacing (HISP) and left bundle area pacing (LBAP) may normalize atrioventricular (AV) conduction with a narrow combination of the Q wave, R wave and S wave (QRS complex) in functional bundle branch block or conduction delay in patients with heart failure (HF).

NCT ID: NCT02711748 Recruiting - Bradycardia Clinical Trials

Can Medical Personnel Properly Proceed in the Case of a Patient With Bradycardia?

Start date: February 2016
Phase: N/A
Study type: Interventional

The study aims to assess the regularity of the proceedings in the case of a patient with bradycardia ECG.

NCT ID: NCT02436616 Recruiting - Premature Birth Clinical Trials

microEEG for Neonatal Apnea, Bradycardia and Desaturation

Start date: January 2013
Phase: N/A
Study type: Observational

The study utilizes microEEG (a novel miniaturized, FDA approved EEG device) to prospectively investigate the cerebral electrical activity of infants with Apnea, Bradycardia and Desaturation events. This project will also assess the feasibility of using the microEEG device in the Neonatal Intensive Care Unit (NICU) setting and the feasibility of remote centralized interpretation in this setting.

NCT ID: NCT02083952 Recruiting - Clinical trials for Gastroesophageal Reflux

Impact of Swaddle Blanket on Gastroesophageal Reflux

Start date: February 2014
Phase: N/A
Study type: Interventional

Gastroesophageal reflux disease (GERD) has been reported in up to 85% of all infants born prematurely, and has been associated with a wide range of symptoms. These include irritability, pauses in breathing, heart rate drops, declines in oxygen levels, chronic lung disease, and delays in growth and development. A novel approach to the mangement of GERD in infants is the use of an abdominal band, applying gentle pressure and possibly reducing the reflux of acid from the stomach. The purpose of this study is to evaluate the impact of a swaddle blanket with an abdominal band insert on the incidence of infant apnea, bradycardia, oxygen declines, and pH (acid) changes.

NCT ID: NCT01825473 Recruiting - Clinical trials for Gastroesophageal Reflux

Study of Erythromycin in GER-Associated Apnea of the Newborn

SEGAN
Start date: September 2012
Phase: N/A
Study type: Interventional

To evaluate the relationship of reflux and apnea and to determine whether the administration of erythromycin improves the incidence of GER and GER-associated apnea, bradycardic and/or desaturation events in a prospective randomized controlled trial.

NCT ID: NCT01755780 Recruiting - Hypotension Clinical Trials

Effect of the Side of Interscalene Block on Bradycardia and Hypotension in Beach Chair Position

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

The Left interscalene block has a different effect on heart's autonomic nervous system, compared to Right interscalene block. This effect is evident on the occurrence of bradycardia and hypotension during shoulder surgery in the beach chair position

NCT ID: NCT01717495 Recruiting - Clinical trials for Cardiovascular Disease

Thromboembolic Complications After Pacemaker or Implantable Cardioverter-Defibrillator Procedures

Start date: April 2013
Phase: N/A
Study type: Observational

This is a large prospective registry of patients submitted to cardiac electronic devices implantation designed to investigate the incidence, risk factors and prognostic of thromboembolic complications associated with transvenous lead implantation.

NCT ID: NCT01717469 Recruiting - Clinical trials for Cardiovascular Disease

Safety and the Effects of Isolated Left Ventricular Pacing in Patients With Bradyarrhythmias

SAFE-LVPACE
Start date: June 2012
Phase: Phase 4
Study type: Interventional

Previous experimental and clinical studies have consistently suggested that right ventricular (RV) apical pacing has important adverse effects. Ventricular pacing, however, is required, and cannot be reduced in many patients with atrioventricular block. The SAFE-LVPACE study is a randomized controlled trial that compare the effects of conventional right ventricular (RV) pacing vs. left ventricular (LV) in patients with AV block.

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.