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Tachycardia clinical trials

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NCT ID: NCT05454137 Recruiting - Clinical trials for Postural Orthostatic Tachycardia Syndrome

A Shared Medical Appointment Intervention for Quality of Life Improvement in POTS

Start date: November 1, 2023
Phase: N/A
Study type: Interventional

Postural orthostatic tachycardia syndrome (POTS) is a clinical syndrome encompassing a myriad of debilitating symptoms that does not have any FDA approved drug therapies. We propose a shared medical appointment intervention where participants will learn lifestyle management therapies and integrative practices that may improve quality of life.

NCT ID: NCT05439031 Recruiting - Clinical trials for Ventricular Tachycardia

StereoTactic Arrhythmia Radiotherapy in the NetherLands no. 2

STARNL-2
Start date: May 19, 2023
Phase: N/A
Study type: Interventional

Ventricular tachycardia (VT) is a malignant cardiac arrhythmia subjecting our patients to a high risk of sudden death, increased morbidity and reduced quality of life. Unfortunately, failure of treatment is common and VT recurrences remain an important concern. In these patients, stereotactic arrhythmia radiotherapy appears to be an effective and safe treatment. The mechanism of action however remains unknown and should be elucidated. The objective of this phase 2, single arm, monocenter, pre-post intervention study is to evaluate the efficacy and safety of stereotactic arrhythmia radiotherapy and obtain insights in the mechanism of action by evaluating electro-anatomical alterations of stereotactic arrhythmia radiotherapy in patients with therapy refractory ventricular tachycardia.

NCT ID: NCT05434650 Recruiting - Atrial Arrhythmia Clinical Trials

Abbott Atrial Fibrillation Post Approval Study

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

This post-approval study is designed to provide continued real-world clinical evidence to confirm the safety and long-term effectiveness of atrial fibrillation (AF) radiofrequency (RF) technologies (e.g. TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™ (TactiCath SE)) for the treatment of AF.

NCT ID: NCT05421208 Recruiting - Long COVID Clinical Trials

Cardiovascular Autonomic and Immune Mechanism of Post COVID-19 Tachycardia Syndrome

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

The term post-acute COVID-19 syndrome or Long COVID is a disabling syndrome that persists beyond the 3-month convalescence period after COVID-19 infections. This syndrome affects mostly women (~80%), present with chronic tachycardia and Orthostatic intolerance symptoms without any identifiable cause. In addition, non-specific symptoms such as fatigue, headache, and "brain fog", commonly described in POTS patients are also present in this novel condition, recently named post-COVID-19 tachycardia syndrome, POTS variant. Reduced Vagal activity and unresolved inflammation is post-COVID-19 POTS is hypothesized as the cause of Long COVID

NCT ID: NCT05410860 Recruiting - Clinical trials for Tachycardia, Supraventricular

Efficacy and Safety Study of Etripamil Nasal Spray Self-Administration for the Termination of Spontaneous Episodes of Paroxysmal Supraventricular Tachycardia

Start date: June 30, 2022
Phase: Phase 3
Study type: Interventional

To determine whether etripamil nasal spray (NS) self-administered by Chinese patients is superior to placebo at terminating episodes of PSVT in an at-home setting; To evaluate the efficacy of etripamil NS self-administered by Chinese patients compared with placebo on a range of clinical markers. To evaluate the safety of etripamil NS self-administered by Chinese patients compared with placebo

NCT ID: NCT05377931 Recruiting - COVID-19 Clinical Trials

Ocular and Cardiac Effects of Battle Ground

Start date: May 10, 2022
Phase:
Study type: Observational

Mobile battle ground games are widely used in various age groups, there are ocular and cardiac affection that may affect users of this type of action games.

NCT ID: NCT05377216 Recruiting - Clinical trials for Ventricular Tachycardia

Characterization of Cardiac Electrophysiological Effects of Autonomic Neuromodulation

Start date: September 1, 2022
Phase: Early Phase 1
Study type: Interventional

Prospective cohort study evaluating the electrophysiologic and biochemical effects of stellate ganglion block in patients with ventricular tachycardia.

NCT ID: NCT05375968 Recruiting - Clinical trials for Postural Tachycardia Syndrome (POTS)

Splanchnic Venous Capacitance in Postural Tachycardia Syndrome

Start date: February 25, 2023
Phase: N/A
Study type: Interventional

Postural tachycardia syndrome (POTS) affects ≈3 million young people, characterized by chronic presyncopal symptoms characterized by dizziness, lightheadedness, and orthostatic tachycardia that occur while standing. Across-sectional survey found that 25% of these patients complains that meals rich in carbohydrates are among the factors that further exacerbate POTS's symptoms and cause a myriad of gastrointestinal symptoms. The splanchnic circulation is the largest blood volume reservoir of the human body, storing ≈25% of the total blood volume and contributing to sudden, and large, fluctuations in the stroke volume (SV). These orthostatic changes in systemic hemodynamics are particularly magnified after meals, due to increased blood volume sequestration triggered by the release of gastrointestinal peptides with vasodilatory properties. The purpose of this study is to determine if the worsening orthostatic tachycardia and symptoms after glucose ingestion in POTS patients are due to a greater increase in splanchnic venous capacitance and excessive blood pooling on standing as compare to Healthy controls

NCT ID: NCT05344599 Recruiting - Clinical trials for Postural Orthostatic Tachycardia Syndrome

Evaluating the Prevalence of Acute Hepatic Porphyria in Postural Tachycardia Syndrome

Start date: January 19, 2022
Phase:
Study type: Observational

Postural Tachycardia Syndrome (POTS) is the most common autonomic disorder and is estimated to affect 3,000,000 individuals in the United States, with 80-85% of patients being women. The condition is characterized by a rapid increase in heart rate (HR) that occurs on standing, and chronic symptoms of cerebral hypoperfusion leading to lightheadedness, dizziness, and blurred vision. The acute hepatic porphyrias(AHP)are among the diseases that present with autonomic cardiovascular(tachycardia)and neurovisceral symptoms (abdominal pain) among others; they present with acute exacerbations Given that there is available treatment for AHP that change the natural progression of the disease, study focuses to investigate the occurrence of AHP in POTS and determine the clinical and neuro-hormonal characteristic of the POTS subgroup that will likely benefit from AHP screening. This study has one visit that involves, answering some questionnaires, coming to the lab for blood work, genetic testing, and some autonomic function tests. About 50 people will take part in this study.

NCT ID: NCT05296954 Recruiting - Clinical trials for Supraventricular Tachycardia

Localization of Anatomical Structures Involved in Nodal Tachycardias by High Density Mapping.

KOCH-MAPPING
Start date: February 4, 2022
Phase: N/A
Study type: Interventional

The aim of the present work is to analyze the capacity of high resolution mapping systems to determine the precise location of the AV node and peri-nodal slow-conducting pathways, using standard recording parameters, but also off-line additional filter changes and additional techniques (conduction velocities, isochrones and dV/dt). The investigative team plan a prospective monocentric study. Detailed high resolution mapping of the Koch triangle and neighboring areas will be collected through the RHYTHMIA HDx 3D electro-anatomical mapping system and the multipolar ORION catheter. This sample will consist of 2 groups of patients: the first will include patients referred for AVNRT ablation and the second will include control patients (without AVNRT), referred for another indication requiring similar mapping system. If visualized, position of the slow pathway and AV node will be compared with the ablation areas, which will be set conventionally under fluoroscopy.