Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D001145', 'term': 'Arrhythmias, Cardiac'}], 'ancestors': [{'id': 'D006331', 'term': 'Heart Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'CASE_CONTROL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 28}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2009-06'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2010-02', 'completionDateStruct': {'date': '2009-11', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2010-02-02', 'studyFirstSubmitDate': '2009-06-10', 'studyFirstSubmitQcDate': '2009-06-11', 'lastUpdatePostDateStruct': {'date': '2010-02-04', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2009-06-12', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2009-11', 'type': 'ACTUAL'}}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'conditions': ['Arrhythmias']}, 'descriptionModule': {'briefSummary': 'Prospective, multicenter, non-randomized study to determine the performance of NUVANT Mobile Cardiac Telemetry system in arrhythmia detection.', 'detailedDescription': 'Arrhythmia patients will be externally monitored. The collected information will be used to evaluate the NUVANT MCT system.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Remote cardiac monitoring', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* 18 years of age or older\n* Patients undergoing remote ambulatory electrocardiographic monitoring\n\nExclusion Criteria:\n\n* Is participating in another clinical study that may confound the results of this study'}, 'identificationModule': {'nctId': 'NCT00919568', 'briefTitle': 'Monitoring Arrhythmia Patients (IMPACT)', 'organization': {'class': 'INDUSTRY', 'fullName': 'Corventis, Inc.'}, 'officialTitle': 'Arrhythmia Detection With Adherent Patient Monitoring', 'orgStudyIdInfo': {'id': 'COR-2009-005'}}, 'contactsLocationsModule': {'locations': [{'zip': '43952', 'city': 'Steubenville', 'state': 'Ohio', 'country': 'United States', 'facility': 'Dr. Bedi', 'geoPoint': {'lat': 40.36979, 'lon': -80.63396}}], 'overallOfficials': [{'name': 'Imad Libbus, PhD', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Corventis, Inc.'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Corventis, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'oldNameTitle': 'Madhuri Bhat, VP Clinical and Regulatory affairs', 'oldOrganization': 'Corventis'}}}}