Clinical Trials Logo

Arrhythmia, Cardiac clinical trials

View clinical trials related to Arrhythmia, Cardiac.

Filter by:

NCT ID: NCT05563701 Completed - Heart Diseases Clinical Trials

Evaluation of the LVivo Image Quality Scoring (IQS)

Start date: September 5, 2022
Phase:
Study type: Observational

The study includes two parts: Part 1: - 100 examinations of patient referred for echo evaluation, containing clips that were acquired from the 4CH apical view were collected retrospectively. Each study includes 10 clips that represent typical user scanning errors - Offline evaluation of the system (by batch processing) shall be performed by comparing the system output to preliminary quality tagging by experienced sonographers Part 2: - Live scans of apical 4CH clips of patients with indication for POCUS examination will be performed by POC physicians - LVivo IQS shall be used (on Lumify) during the scan for patients that meet inclusion criteria until 50 exams will be collected. 3 sec of each scan shall be saved, and Image quality score (IQS) shall be documented - Saved scans shall be reviewed by an expert physician to determine whether they are clinically interpretable

NCT ID: NCT05437926 Recruiting - Arrhythmia, Cardiac Clinical Trials

A Study to Describe the Effectiveness of Arrhythmia Analysis Software for Screening of Sinus Rhythm, Atrial Fibrillation and Premature Beats in light-and Dark Skin Tone Patients

Start date: April 21, 2022
Phase:
Study type: Observational

The purpose of this study is to describe the Huawei'ssoftware ("Arrhythmia Analysis Software") for the detection of atrial fibrillation, premature beats, and sinus rhythm using photoplethysmography (PPG). Data derived from a wearable device with a PPG sensor (watch or band) in patients with light skin or dark skin tones will be used as an index test. The Huawei software is intended as a pre-screening technology. It should identify candidates who may benefit from further evaluation. The software is not intended to be a diagnostic system.

NCT ID: NCT04345627 Recruiting - Arrhythmia, Cardiac Clinical Trials

Japanese Lead Extraction Registry

J-LEX
Start date: July 1, 2018
Phase:
Study type: Observational [Patient Registry]

Japanese Lead Extraction (J-LEX) Registry is an observational nationwide registry, performed by Japanese Heart Rhythm Society, collaborated with the National Cerebral and Cardiovascular Center. The acute success rate at discharge and the complications associated with transvenous lead extraction will be collected. J-LEX registry will provide a reliable information on indications, methods, the success rate, complications and the prognosis at 30 days prognosis.

NCT ID: NCT04076020 Completed - Atrial Fibrillation Clinical Trials

Atrial Fibrillation Health Literacy and Information Technology Trial in Rural PA Counties

AFibLITT_R
Start date: January 8, 2020
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is a highly prevalent, morbid condition. Anticoagulation to prevent thromboembolic strokes is a foremost priority in AF but adherence is challenging for patients and lapses in anticoagulation are common. Chronic disease self-management (CDSM) is a recognized program to enhance self-efficacy and improve adherence, quality of life, and patient-centered health outcomes. Rural patients with AF experience increased vulnerability to adverse outcomes due to geographic and social isolation, poor health care access, and limited health literacy. This study uses an innovative, scalable CDSM intervention to improve anticoagulation adherence in rural patients with AF.

NCT ID: NCT03647891 Suspended - Heart Failure Clinical Trials

Impact of Early Diagnosis and Treatment of OSA on Hospital Readmission in Hospitalized Cardiac Patients

CV Readmit
Start date: July 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether early diagnosis of obstructive sleep apnea and initiation of and adherence to CPAP therapy in hospitalized cardiac patients would impact 30-day hospital readmission rates.

NCT ID: NCT03150030 Completed - Clinical trials for Diabetes Mellitus, Type 2

Hypoglycaemia and Cardiac Arrhythmias in Type 2 Diabetes

HYPO-HEART
Start date: February 1, 2017
Phase:
Study type: Observational

Twenty-one patients with insulin-treated type 2 diabetes with diabetic complications will be recruited to Part 1 of the study, a three-hour combined hyper- and hypoglycaemic clamp, along with a control group of twenty-one individuals with normal glucose tolerance matched for age, gender, and body mass index. Patients with type 2 diabetes will be scheduled for a three-week run-in period with LR and CGM prior to participation in Part 1. Only patients with a well-functioning loop-recorder and who can comply with CGM will be included. Patients with type 2 diabetes will continue in part 2 of the study, a one year observational study employing CGM and LR and clinical examination after 1, 3, 6, 9, and 12 months and an extended observation period of 2 years employing LR and clinical examination.

NCT ID: NCT03035227 Terminated - Arrhythmia, Cardiac Clinical Trials

Catheter Ablation of Arrhythmias to Improve CRT Response

ABLATE-CRT
Start date: January 23, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test if catheter ablation is better than medication therapy at treating arrhythmias originating from the upper and/or lower chambers of the heart in order to allow the heart to beat properly.

NCT ID: NCT02991716 Completed - Arrhythmia, Cardiac Clinical Trials

Surface Electrocardiogram (ECG) Signal Recording for Implantable Subcutaneous String Defibrillator (ISSD) Development

Start date: January 2016
Phase: N/A
Study type: Observational

Record cutaneous Electrocardiogram (ECG) data from positions corresponding to the expected subcutaneous locations of the Implantable Subcutaneous String Defibrillator (ISSD) using existing, approved ECG recording devices.

NCT ID: NCT02988219 Recruiting - Surgery Clinical Trials

Cardiac Arrhythmias in Patients Undergoing Kidney Cancer Surgery Depending on the Anaesthesia Method

Start date: June 2010
Phase: Phase 4
Study type: Interventional

This study evaluates the incidence of cardiac arrhythmias during the perioperative period in patients undergoing open kidney cancer surgery in the lateral position. All the participants will be randomly allocated to receive general (Group G) or combined epidural/general anaesthesia (Group G/E). The anaesthetic technique is standardized. The Holter monitor will be applied at the evening before the surgery, tracing continuously for a period of 24 hours (7PM-7PM)

NCT ID: NCT02585817 Completed - Arrhythmia, Cardiac Clinical Trials

Remote Patient Management for Cardiac Implantable Electronic Devices

RPM-CIED
Start date: October 2016
Phase: N/A
Study type: Interventional

This is a pilot study to assess barriers, evaluate and implement a patient oriented CIED management model incorporating advanced technological innovation to promote a paradigm shift to patient-centered care involving remote CIED monitoring and programming. The advancement in technology is very important as it addresses several potential gaps and barriers in the care of patients with CIEDS: 1. Long, expensive travel for patients 2. Morbidity to patients due to delay in receiving appropriate treatment 3. Efficiency in health care delivery 4. Patient satisfaction