CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 262 enrolled
Drug / intervention
MRI Scanother
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.

Search/NCT02318550
NCT02318550N/ACompleted
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A Single Institution Registry Trial Evaluating the Safety of MRI for Patients With Non-MRI Conditional Pacemakers and ICD

Lancaster General Hospital·observational·Posted Dec 17, 2014·Updated Aug 31, 2021

In Brief

An observational study evaluating MRI Scan for MRI Scans and 3 related conditions. Completed, enrolled 262 participants across 1 site.

Detailed Summary

The purpose of the registry is to accumulate pre-and post-scan device interrogation data for the purpose of determining the risk of MRI for patients with implantable devices.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsMRI Scans, Magnetic Resonance Imaging, Pacemaker, Implantable Cardioverter Defibrillator
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedDec 17, 2014
Enrollment StartDec 1, 2014
Primary CompletionJun 30, 2018
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 11.5 years ago

Interventions

MRI Scanother

The MRI will be performed with a 1.5 T scanner utilizing institutional protocols and the following settings: * Normal operating mode * SAR ≤ 2.0 W/kg per patient.