At a glance
ClinicalIndex Comparison RecordN/ACompleted· 322 enrolled
Drug / intervention
Jewel Patch Wearable Cardioverter Defibrillator (P-WCD)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Clinical Evaluation of the Jewel P-WCD in Subjects at High Risk for Sudden Cardiac Arrest
In Brief
A clinical study evaluating Jewel Patch Wearable Cardioverter Defibrillator (P-WCD) for Sudden Cardiac Arrest. Completed, enrolled 322 participants across 30 sites.
Detailed Summary
The Jewel IDE Study: A Clinical Evaluation of the Jewel P-WCD in Subjects at High Risk for Sudden Cardiac Arrest. ("JEWEL")
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSudden Cardiac Arrest
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
Enrollment StartJan 2022
First PostedJan 2022
Primary CompletionNov 2023
TodayJul 2026
First PostedJan 21, 2022
Enrollment StartJan 12, 2022
Primary CompletionNov 10, 2023
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 4.4 years ago
Interventions
Jewel Patch Wearable Cardioverter Defibrillator (P-WCD)device
Automatic external cardioverter defibrillator that monitors patients at risk for SCA and provides a therapeutic shock if needed.