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Arrhythmias, Cardiac clinical trials

View clinical trials related to Arrhythmias, Cardiac.

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NCT ID: NCT04837495 Completed - Pain, Acute Clinical Trials

Stellate Ganglion Block in Control of Arrhythmia in Laparoscopic Cholecystectomy

Start date: April 30, 2021
Phase: N/A
Study type: Interventional

During Laparoscopic cholecystectomy, carbon dioxide (CO2) pneumoperitoneal laparoscopic surgery, CO2-pneumoperitoneum activates the sympathoadrenomedullary system to increase the release of catecholamines such as epinephrine (E) norepinephrine (NE) and dopamine (DA). During stress, E and NE are secreted by the adrenal medulla into blood circulation to promote glycogenolysis to increase blood glucose, speed up lipolysis and accelerate heartbeats. Stellate g anglion block (SGB) reters to the blockade of sympathetic nerves including the large area covered by middle cervical, vertebral arterial. stellate ganglions and ther pre- and post- ganglions. SGB affects both peripheral and central nervous systems. In the peripheral system. the sympathetic pre- and post-ganglionic fibers in the innervated areas of stellate ganglion are affected. Therefore, the control of vascular dilatation and constriction, muscular movement, bronchial smooth muscle relaxation and contraction, and pain conduction, by sympathetic nerves is inhibited. In the central nervous system, the hypothalamus is mainly involved in the regulation of systemic autonomic nervous, immune and endocrine systems, and to maintain homeostasis. CO2-pneumoperitoneum causes severe stress-related homeostatic disorders including arrhythmia and blood pressure changes. This study will examine the effects of stellate ganglion block (SGB) on hemodynamics and stress response in patients undergoing CO-pneumoperitoneal surgery.

NCT ID: NCT04833712 Recruiting - Clinical trials for Cardiovascular Diseases

Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation

RAD-AF
Start date: May 10, 2021
Phase: N/A
Study type: Interventional

The study aims to investigate the short-term (3 months) and intermediate-term (12 months) safety and preliminary efficacy of stereotactic radiotherapy for pulmonary vein isolation to treat refractory atrial fibrillation.

NCT ID: NCT04818697 Completed - Covid19 Clinical Trials

Effect of Social Isolation on Physical Activity Level, and Kinesophobia in Heart Rhythm Disorders During Pandemic

Start date: June 24, 2020
Phase:
Study type: Observational

The aim of our study is to examine the effect of social isolation on physical activity level, health literacy and kinesophobia in heart rhythm disorders.

NCT ID: NCT04809701 Completed - Clinical trials for Ventricular Arrythmia

Non-vascular ICD Electrode Configuration Feasibility Study

Start date: March 22, 2021
Phase: N/A
Study type: Interventional

This study is designed to evaluate the energy requirements of two different Nonvascular ICD (NV-ICD) electrode configurations for achieving successful defibrillation of ventricular arrhythmias.

NCT ID: NCT04776642 Recruiting - Arrythmia Clinical Trials

Biobank for "Arrhythmia and Conduction Disorders: TowArd Pathophysiology Based Treatment"

ADAPT
Start date: December 18, 2014
Phase:
Study type: Observational [Patient Registry]

The 'ADAPT' Biobank is a collection of body material and data from patients with or at risk of cardiac arrhythmias who underwent or will undergo (non-) invasive treatment for this disease. Its main objective is to obtain a comprehensive collection of patient information and material to facilitate research and gain better insight into the complex pathophysiology of the different arrhythmias, the multifactorial process, the heterogeneity in clinical presentation, and prognosis. Bodily material is used for biochemical marker assessments, histological and molecular analyses for research in cardiac arrhythmias.

NCT ID: NCT04774523 Recruiting - Heart Failure Clinical Trials

Evaluation of the BIOTRONIK AutoAdapt Algorithm for Continuous Automatic Adaptive Cardiac Resynchronization

BIO|Adapt
Start date: August 31, 2021
Phase: N/A
Study type: Interventional

BIO|Adapt study is designed to provide evidence for the clinical benefit of the CRT AutoAdapt feature. This feature provides continuous adaptation of AV delay and biventricular pacing modality. However, additional clinical data on the short and mid-term improvement of CRT-D patients by the CRT AutoAdapt feature are needed.

NCT ID: NCT04754204 Completed - Cardiac Arrhythmia Clinical Trials

Mobile Cardiac Telemetry and Advanced Multi-Parameter Monitoring in Patients

MAPS
Start date: December 15, 2020
Phase:
Study type: Observational

To determine the associations among biometric data, arrhythmias, subject-reported symptoms and subject wellness.

NCT ID: NCT04750798 Recruiting - Cardiac Arrhythmias Clinical Trials

An Observational Post-marketing Study Using Commercially Approved Biosense Webster (BWI) Medical Devices for the Treatment of Participants With Cardiac Arrhythmias

Start date: February 22, 2021
Phase:
Study type: Observational

The purpose of this study is to prospectively collect clinical data evaluating the ongoing safety and performance during routine-use standard cardiac arrhythmia mapping and/or ablation procedures while using commercial Biosense Webster Inc. (BWI) medical devices. Data generated from the study will be used to confirm safety and performance of BWI medical devices in the marketed phase and to expand the body of evidence on the use of these devices and techniques in treatment of cardiac arrhythmias.

NCT ID: NCT04735016 Recruiting - Arrhythmia Clinical Trials

DiamondTemp Global Registry

Start date: April 22, 2021
Phase:
Study type: Observational [Patient Registry]

The DiamondTemp™ Global Registry is a prospective, global, multi-center, observational post-market registry.

NCT ID: NCT04727645 Recruiting - Cardiac Arrhythmia Clinical Trials

Use of "iSuite" During CMR-guided Electrophysiological Procedures

Start date: January 4, 2021
Phase:
Study type: Observational

The perpuse of this study is to investigate the feasibility of the Philips interventional MRI suite "iSuite" to create an electroanatomical map of the heart based on which the real-time location of the catheters can be correctly and reliably visualized during CMR-guided electrophysiological procedure (CMR-EP).