Superficial Cervical Plexus Block for Pacemaker Insertion

Stopped early · Not applicable

Conditions studied: Pacemaker Insertion, Regional Block, Pain

In brief

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.

Key facts

Study ID

NCT01473667

Run by

Mayo Clinic

People needed

30

Starts

2011-11-01

Expected to finish

2016-09-01

Last updated by the study team

2019-02-01

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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

You may not qualify if…

• 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

Where it is running

• Mayo Clinic — Jacksonville, Florida, United States

Full record on ClinicalTrials.gov

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