Viewing Study NCT00170261



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00170261
Status: COMPLETED
Last Update Posted: 2018-04-05
First Post: 2005-09-12

Brief Title: ELIAS Early Loop-Recorder in Suspected Arrhythmogenic Syncope
Sponsor: Medtronic Bakken Research Center
Organization: Medtronic Bakken Research Center

Study Overview

Official Title: Early Loop-Recorder in Suspected Arrhythmogenic Syncope
Status: COMPLETED
Status Verified Date: 2018-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a prospective controlled opened randomized study to evaluate the cost benefit of a primary implantation of a loop recorder versus the conventional diagnostic cascade for syncope most likely due to cardiac arrhythmia
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None