Viewing Study NCT01473667


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Study NCT ID: NCT01473667
Status: TERMINATED
Last Update Posted: 2019-02-01
First Post: 2011-11-14
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Superficial Cervical Plexus Block for Pacemaker Insertion
Sponsor: Mayo Clinic
Organization:

Study Overview

Official Title: Superficial Cervical Plexus Block for Pacemaker Insertion
Status: TERMINATED
Status Verified Date: 2019-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: change in practice occured
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to investigate clinical outcomes from two current standard of care pain control procedures performed for patients undergoing pacemaker insertion.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: