Superficial Cervical Plexus Block for Pacemaker Insertion

Not Applicable

Terminated

• Conditions: Pain; Pacemaker Insertion; Regional Block
• Interventions: Procedure: Local site infiltration; Procedure: Superficial Cervical Plexus Block (SCP) block

• Registration Number: NCT01473667
• Lead Sponsor: Mayo Clinic

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

Not available

Study Timeline

• Study Start: 2011-11
• Study First Submitted: 2011-11-14
• Study First Submitted QC: 2011-11-16
• Study First Posted: 2011-11-17
• Primary Completion: 2015-03
• Study Completion: 2016-09
• Status Verified: 2019-01
• Last Update Submitted: 2019-01-31
• Last Update Posted: 2019-02-01

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Age 18-100 years old
• Registered patients at Mayo Clinic in Florida scheduled to undergo primary insertion of pacemaker

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Exclusion Criteria

• Emergency placement of pacemaker
• Sub-pectoral placement of pacemaker
• Patients with history of chronic pain
• Patients with anatomical abnormality or disruption to the pacemaker insertion site or site of block placement
• Patients with allergy to local anesthetic

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Local Infiltration	Local site infiltration	-
Superficial Cervical Plexus Block	Superficial Cervical Plexus Block (SCP) block	-

Primary Outcome Measures

Name	Time	Method
To decrease opioid requirements after Pacemaker insertion	first 24 hrs post pacemaker insertion

Trial Locations

Locations (1)

Mayo Clinic; 🇺🇸 Jacksonville, Florida, United States