Clinical Validation of a Cardiovascular Autonomic Nervous Function Multi-Parameter Evaluation System
NCT06447896 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 235
Last updated 2024-06-10
Summary
This is a open-label, randomized, paired design, multicenter study of the Cardiovascular Autonomic Nervous Function Multi-Parameter Evaluation System (R6000) for evaluating cardiovascular autonomic neuropathy. R6000 is novel intellectual diagnostic device for cardiovascular autonomic reflex tests and heart rate variability analysis. A total of 85 subjects will be enrolled in trial Ⅰ and 150 subjects will be enrolled in trial Ⅱ. In trial Ⅰ, subjects will be randomized to two groups, one of which will receive test by the tested device first and the other one will be tested by conventional blood pressure kit. The primary objective of this clinical trial is to evaluate the effectiveness of the Cardiovascular Autonomic Nervous Function Multi-Parameter Evaluation System. The secondary objective is to evaluate the safety of the cardiovascular autonomic testing system and stability.
Conditions
- Cardiovascular Autonomic Neuropathy
Interventions
- DEVICE
-
Cardiovascular Autonomic Nervous Function Multi-Parameter Evaluation System (Model: R6000)
Cardiovascular autonomic reflex tests (CARTs) and heart rate variability analysis (HRV) are conducted with Cardiovascular Autonomic Nervous Function Multi-Parameter Evaluation System (Model: R6000). CARTs include five standardized tests, which are heart rate response to lying-to-standing, Valsalva maneuver, deep breathing, and blood pressure response to lying-to-standing and sustained isometric handgrip. These series of movements act as "standardized stimuli" to trigger hemodynamic changes in the body, altering vagal and sympathetic activity through mechanisms such as the baroreflex, thereby producing changes in heart rate and blood pressure. The sensor-monitoring interactive design of the device ensures the standardization of these maneuvers.
- DIAGNOSTIC_TEST
-
Conventional method of CARTs
Conventional method are conduced using blood pressure kit with manual sphygmomanometer and ECG machine. Conventional method and the investigated device are used simultaneously to record electrocardiograms. Conventional blood pressure taking are carried out in sequence with the investigated device. CARTs results from the conventional method are used as control.
- DEVICE
-
Ambulatory holter station Model i12 plus
Model i12 plus (manufactured by RENCARE) is an ambulatory holter station, which was approved by the Center for Medical Device Evaluation (CMDE), China National Medical Products Association (NMPA). It can analyze electrocardiogram and generate HRV indices, which include SDNN, RMSSD, NN50, pNN50, triangular index, average RR, deceleration capacity (DC), deceleration runs (DRs), VLF, LF, HF, LF/HF, and total power. Model i12 plus is used to analyzed the same ECG signals as the investigated device.
Sponsors & Collaborators
-
REEM (Shenzhen) Healthcare Co., Ltd
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2011-03-11
- Primary Completion
- 2022-08-12
- Completion
- 2022-08-12
More Related Trials
-
Sympathetic Nerve Activity and an Implantable Cardioverter Defibrillator in Heart Failure Patients
NCT00439790 ·Status: COMPLETED
-
MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post MI Patients
NCT00305214 ·Status: COMPLETED ·Phase: NA
-
Chronic Evaluation of Novel Pacemaker System
NCT06056817 ·Status: RECRUITING ·Phase: NA
-
Corheart 6: Long-term Cohort Study
NCT07094919 ·Status: RECRUITING ·Phase: NA
-
RAMP 200 / RAMP Cardiovascular Tests at the Point-of-Care
NCT02191735 ·Status: COMPLETED
-
Cardiac Output Autonomic Stimulation Therapy for Heart Failure - Hemodynamic Effects
NCT03542123 ·Status: UNKNOWN ·Phase: NA
-
Atrial Fibrillation Rate Control Therapy Guided By Continuous Ambulatory Monitoring
NCT00115843 ·Status: WITHDRAWN ·Phase: NA
-
Electrical Optimization of Cardiac Resynchronization Therapy in Non-responder Patients
NCT03789487 ·Status: TERMINATED ·Phase: NA
-
Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac Autonomic Dysfunction
NCT02594488 ·Status: COMPLETED ·Phase: NA
-
Optimal Pacing Rate for Cardiac Resynchronization Therapy
NCT06445439 ·Status: RECRUITING ·Phase: NA
-
MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post MI Patients
NCT00305240 ·Status: COMPLETED ·Phase: NA
-
ConTempoRary Cardiac Stimulation in Clinical practicE: lEft, BivEntriculAr, Right, and conDuction System Pacing
NCT06324682 ·Status: RECRUITING
-
Full Early Atrial Diagnostics in Single Chamber ICD Patients Using the DX Lead and Home Monitoring in Brazil.
NCT04869527 ·Status: COMPLETED
-
AI Powered Mapping Technology for Identifying Arrhythmias
NCT06939478 ·Status: COMPLETED
-
Applying an Artificial Intelligence-Enabled Electrocardiographic System for Reducing Mortality
NCT05118035 ·Status: COMPLETED ·Phase: NA
-
REVEAL for Respiration Detection
NCT01956578 ·Status: UNKNOWN ·Phase: NA
-
Factors Affecting Selection of Leadless Pacemaker and Atrioventricular Synchronous Pacing Status
NCT06587672 ·Status: NOT_YET_RECRUITING
-
Remote Monitoring in Patients With Heart Failure
NCT04537104 ·Status: UNKNOWN
-
Observation of ImageReady™ MR Conditional Pacing System in China
NCT02636712 ·Status: COMPLETED
-
Development of a Novel Convolution Neural Network for Arrhythmia Classification
NCT03662802 ·Status: COMPLETED
-
Zero-fluoroscopic Navigation Versus Conventional Fluoroscopic Navigation for Double-chamber Pacemaker Implantation
NCT03118427 ·Status: UNKNOWN ·Phase: NA
-
Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-approval Study
NCT02849769 ·Status: COMPLETED
-
Safety and Performance Evaluation of a New Catheter Range for Lead Implantation At Interventricular Septum
NCT06453850 ·Status: RECRUITING ·Phase: NA
-
CRT RENEWAL Registry
NCT00146874 ·Status: COMPLETED
-
MAgnetic Resonance Imaging-guided implanTation of Cardioverter DEFibrillators
NCT06269692 ·Status: NOT_YET_RECRUITING ·Phase: NA