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Bradycardia clinical trials

View clinical trials related to Bradycardia.

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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: NCT01819064 Completed - Bradycardia Clinical Trials

Heart Rate Response to Atropine Doses Less Than 0.1mg IV to Anesthetized Infants

Start date: February 2013
Phase: Phase 4
Study type: Interventional

An infants heart rate is very important because it ensures that blood is pumped to all organs in the body. Heart rate may decrease during anesthesia and surgery, and this is why the anesthesiologist will often give a medication to prevent this from happening. The most common drug for this purpose is called atropine. The dose of most drugs given to babies is based upon the baby's weight, but some believe that the dose of atropine should not be less than 0.1mg. However there is no evidence to support this minimum dose. A larger dose of atropine may cause a very fast heart rate instead. Anesthesiologists routinely dose the atropine based upon the baby's weight without regard for a minimum dose. The purpose of the present study is to measure the heart rate after doses of atropine in neonates and infants who receive less than 0.1 mg.

NCT ID: NCT01809652 Completed - Bradycardia Clinical Trials

Feasibility Study of Remote Support for Implantable Pulse Generator (IPG)/Implantable Cardioverter Defibrillator (ICD) Implant

Start date: December 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to gain real world, live implant experience with the remote implant support system. This system is intended to provide the technical support for device implants from a remote location through telepresence (audio and video) and remote control. Specifically, the goals of this study are to corroborate bench testing, assess the performance of the system, gain understanding of the workflows, customer experience, and logistics. The intent of the remote support model is to provide the same support that would typically be provided by a local support person, only remotely. As such, the remote support person would only perform actions that a local support person would routinely do under the direction of a physician. This may involve observing patient data, providing technical support and advice, and performing testing and device reprogramming via remote control of the programmer.

NCT ID: NCT01781078 Completed - Bradycardia Clinical Trials

ImageReady(TM) MR Conditional Pacing System Clinical Study

SAMURAI
Start date: February 2013
Phase: N/A
Study type: Interventional

The objective of the SAMURAI Clinical Study is to collect data to confirm the safety, performance and effectiveness of the ImageReady System for use in the Magnetic Resonance Imaging (MRI) environment when used in accordance with the Conditions of Use included in the Boston Scientific MRI Technical Guide

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: NCT01754064 Completed - Heart Disease Clinical Trials

St. Jude Medical Product Longevity and Performance (SCORE) Registry

Start date: November 2007
Phase:
Study type: Observational

SCORE is an active, prospective, non-randomized, multi-center outcome-oriented registry of patients implanted with St Jude Medical (SJM) market-released cardiac rhythm management (CRM) products. This registry will be conducted in the United States (US). The primary purpose of the registry is to evaluate and publish acute and long-term performance of market-released SJM CRM products by analyzing product survival probabilities. Product status and any related adverse events will be collected to measure survival probabilities.

NCT ID: NCT01750775 Enrolling by invitation - Clinical trials for Premature Ventricular Contraction

Shensongyangxin Capsule in the Treatment of Sinus Bradycardia With Premature Ventricular Contractions

SS-SBVPT
Start date: August 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the effects of Chinese medicine Shansong Yangxin capsule for sinus bradycardia complicated with ventricular premature beats.

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: NCT01715558 Completed - Bradyarrhythmia Clinical Trials

Clinical Outcome of Pacemaker paTIents According to Pacing Modality and Primary INDications OPTI-MIND 2

OPTI-MIND 2
Start date: February 2013
Phase: N/A
Study type: Observational

The purpose of the study is to demonstrate that reduction of unnecessary pacing provided by RYTHMIQ algorithm programed to ON in a pacemaker is associated with better clinical outcomes in bradycardia target population.