At a glance
ClinicalIndex Comparison RecordN/ACompleted· 250 enrolled
Drug / intervention
External Loop Recorderdevice
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.
IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ventricular Function Using External Loop Recorders (INSPIRE-ELR Study)
In Brief
A clinical study evaluating External Loop Recorder for Post MI Left Ventricular Dysfunction. Completed, enrolled 250 participants across 1 site.
Detailed Summary
The purpose of the INSPIRE-ELR study is to characterize arrhythmias in post MI low EF (≤35%) patients in the acute phase (at discharge from hospital after index MI) and chronic phase (at 8-10 weeks after index MI) and to correlate with patients at high risk of all-cause mortality or sudden cardiac death (SCD) at 1 year.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPost MI Left Ventricular Dysfunction
CountriesIndia
CollaboratorsMedtronic
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedNov 2013
Enrollment StartApr 2014
Primary CompletionFeb 2016
Study CompletionApr 2017
TodayJul 2026
First PostedNov 26, 2013
Enrollment StartApr 1, 2014
Primary CompletionFeb 20, 2016
Study CompletionApr 1, 2017
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 12.6 years ago
Interventions
External Loop Recorderdevice