Ignite Creation Date:
2025-12-25 @ 1:39 AM
Ignite Modification Date:
2026-01-25 @ 4:11 AM
Study NCT ID:
NCT03126994
Status:
COMPLETED
Last Update Posted:
2018-08-31
First Post:
2017-04-10
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Prospective, Single-Center, Non-Randomized Study of the PhysioWave™ Cardiovascular Analyzer
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'interventionBrowseModule': {'meshes': [{'id': 'D063177', 'term': 'Pulse Wave Analysis'}], 'ancestors': [{'id': 'D003935', 'term': 'Diagnostic Techniques, Cardiovascular'}, {'id': 'D019937', 'term': 'Diagnostic Techniques and Procedures'}, {'id': 'D003933', 'term': 'Diagnosis'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'OTHER', 'interventionModel': 'SINGLE_GROUP', 'interventionModelDescription': 'Prospective validation study to evaluate PWV, PR, and BW accuracy in a sample of subjects representing the US general adult population.'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 160}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2017-04-11', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2018-08', 'completionDateStruct': {'date': '2017-05-19', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2018-08-29', 'studyFirstSubmitDate': '2017-04-10', 'studyFirstSubmitQcDate': '2017-04-19', 'lastUpdatePostDateStruct': {'date': '2018-08-31', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2017-04-25', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2017-05-19', 'type': 'ACTUAL'}}, 'outcomesModule': {'otherOutcomes': [{'measure': 'Exploratory Analysis: Impact of Strong Vasoactive Drugs on PWV Equivalence', 'timeFrame': 'Day 1', 'description': 'An exploratory analysis will be conducted to evaluate any effects of strong vasoactive drugs, such as those used to control high blood pressure, on equivalency when measuring: pulse wave velocity (PWV) (in m/s) between the PhysioWave Cardiovascular Analyzer and AtCor Medical SphygmoCor® XCEL PWA \\& PWV.'}, {'measure': 'Exploratory Analysis: Impact of BMI on PWV Equivalence', 'timeFrame': 'Day 1', 'description': 'An exploratory analysis will be conducted to evaluate any effect(s) of BMI (in kg/m\\^2) on equivalency when measuring: pulse wave velocity (PWV) (in m/s) between the PhysioWave Cardiovascular Analyzer and AtCor Medical SphygmoCor® XCEL PWA \\& PWV.'}], 'primaryOutcomes': [{'measure': 'Primary Objective: PWV Equivalence', 'timeFrame': 'Day 1', 'description': 'The first primary study objective is to demonstrate equivalency when measuring: pulse wave velocity (PWV) (in m/s) between the PhysioWave Cardiovascular Analyzer and AtCor Medical SphygmoCor® XCEL PWA \\& PWV.'}, {'measure': 'Pulse Rate Equivalence', 'timeFrame': 'Day 1', 'description': 'The second primary study objective is to demonstrate equivalency when measuring: pulse rate (in bpm) between the PhysioWave Cardiovascular Analyzer and AtCor Medical SphygmoCor® XCEL PWA \\& PWV.'}, {'measure': 'Body Weight Equivalence', 'timeFrame': 'Day 1', 'description': 'The third primary study objective is to demonstrate equivalency when measuring body weight (in kg) between the PhysioWave Cardiovascular Analyzer and the Detecto Solo.'}], 'secondaryOutcomes': [{'measure': 'Secondary Objective: BMI Equivalence', 'timeFrame': 'Day 1', 'description': 'Demonstrate equivalency when measuring Body Mass Index (BMI) (in kg/m\\^2) between the PhysioWave Cardiovascular Analyzer and the Detecto Solo'}, {'measure': 'Secondary Objective: Precision Analysis, PWV', 'timeFrame': 'Day 1 or Day 2', 'description': 'Evaluate the precision of PWV measurements (in m/s) due to the sources of variation in measurements in the PhysioWave Cardiovascular Analyzer and AtCor Medical SphygmoCor® XCEL PWA \\& PWV. Sources of variation to be assessed include between-replicates, between-device, between-operator, and total (overall).'}, {'measure': 'Secondary Objective: Precision Analysis, Pulse Rate', 'timeFrame': 'Day 1 or Day 2', 'description': 'Evaluate the precision of pulse rate measurements (in bpm) due to the sources of variation in measurements in the PhysioWave Cardiovascular Analyzer and AtCor Medical SphygmoCor® XCEL PWA \\& PWV. Sources of variation to be assessed include between-replicates, between-device, between-operator, and total (overall).'}, {'measure': 'Secondary Objective: Precision Analysis, Body Weight', 'timeFrame': 'Day 1 or Day 2', 'description': 'Evaluate the precision of body weight measurements (in kg) due to the sources of variation in measurements in the PhysioWave Cardiovascular Analyzer and the Detecto Solo. Sources of variation to be assessed include between-replicates, between-device, between-operator, and total (overall).'}, {'measure': 'Secondary Objective: Precision Analysis, BMI', 'timeFrame': 'Day 1 or Day 2', 'description': 'Evaluate the precision of BMI measurements (in kg/m\\^2) due to the sources of variation in measurements in the PhysioWave Cardiovascular Analyzer and the Detecto Solo. Sources of variation to be assessed include between-replicates, between-device, between-operator, and total (overall).'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': True}, 'conditionsModule': {'conditions': ['Cardiovascular Risk Factor']}, 'descriptionModule': {'briefSummary': 'This is a prospective, single-center, non-randomized validation study being conducted under a non-significant risk study design with the primary aim to evaluate PWV, PR, and BW accuracy in a sample of subjects representative of the US general adult population. The primary study objective is to demonstrate equivalency when measuring: Pulse Wave Velocity (PWV) and Pulse Rate (PR) between the PhysioWave Cardiovascular Analyzer (CA) and AtCor Medical SphygmoCor® XCEL PWA \\& PWV (XCEL), and Body Weight (BW) between the CA and the Detecto Solo Digital Healthcare Scale (Detecto).'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Subjects \\>18 years old\n* Subject signs a written Informed Consent form to participate in the study, prior to any study procedures\n\nSubgroup Inclusion Criteria\n\n* Subject has been taking ACE Inhibitors or Angiotensin Receptor Blockers for at least 30 days\n\nExclusion Criteria:\n\n* Known significant carotid or femoral artery stenosis\n* Non-palpable (non-detectable) arterial pulse at the sites of measurements\n* Pacemaker, defibrillator, or other cardiac stimulator\n* Erratic, accelerated or mechanically controlled irregular heart rhythm, or an arrhythmia\n* History of cardiac valve disorder or cardiac valve disease\n* History of venous disease, including venous insufficiency or deep vein thrombosis\n* History of peripheral artery disease\n* Requirement for supplemental oxygen\n* Neuromuscular disorders that cause shaking or tremors (such as Parkinson's disease or Multiple Sclerosis), or other disease or condition affecting balance\n* Amputation or malformation of any limb or extremity (foot, leg, or arm) which would impede the placement of blood pressure cuffs or standing on the scale with two feet.\n* Known or suspected pregnancy\n* Inability to provide informed consent\n* Mental incompetence or a prisoner status\n* Current participation in a clinical trial of another investigational drug or device in which the study endpoint has not been met\n* BMI \\> 40\n* Subjects \\> 400 lbs\n* Subjects on strong vasoactive drugs, such as those used to control high blood pressure, for \\<30 days\n* Blood loss or blood donation of ˃ 550 mL within 30 days before study procedure"}, 'identificationModule': {'nctId': 'NCT03126994', 'briefTitle': 'Prospective, Single-Center, Non-Randomized Study of the PhysioWave™ Cardiovascular Analyzer', 'organization': {'class': 'INDUSTRY', 'fullName': 'PhysioWave, Inc.'}, 'officialTitle': 'Prospective, Single-Center, Non-Randomized Study of the PhysioWave™ Cardiovascular Analyzer', 'orgStudyIdInfo': {'id': '780-00033'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'PhysioWave Cardiovascular Analyzer', 'description': 'The Experimental Device is the PhysioWave Cardiovascular Analyzer, which will be used to measure Pulse Wave Velocity, Pulse Rate, Body Weight, and BMI. This will be compared to FDA-cleared devices to determine equivalence: AtCor XCEL PWA \\& PWV to measure Pulse Wave Velocity and Pulse rate, and Detecto SOLO to measure Body Weight and BMI.', 'interventionNames': ['Device: PhysioWave Cardiovascular Analyzer', 'Device: AtCor XCEL PWA & PWV', 'Device: Detecto SOLO']}], 'interventions': [{'name': 'PhysioWave Cardiovascular Analyzer', 'type': 'DEVICE', 'description': 'Measurement of Pulse Wave Velocity, Pulse Rate, Body Weight and BMI', 'armGroupLabels': ['PhysioWave Cardiovascular Analyzer']}, {'name': 'AtCor XCEL PWA & PWV', 'type': 'DEVICE', 'description': 'Measurement of Pulse Wave Velocity and Pulse Rate', 'armGroupLabels': ['PhysioWave Cardiovascular Analyzer']}, {'name': 'Detecto SOLO', 'type': 'DEVICE', 'description': 'Measurement of Body Weight and BMI', 'armGroupLabels': ['PhysioWave Cardiovascular Analyzer']}]}, 'contactsLocationsModule': {'locations': [{'zip': '94598', 'city': 'Walnut Creek', 'state': 'California', 'country': 'United States', 'facility': 'Diablo Clinical Research', 'geoPoint': {'lat': 37.90631, 'lon': -122.06496}}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'PhysioWave, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}