Status:
TERMINATED
Superficial Cervical Plexus Block for Pacemaker Insertion
Lead Sponsor:
Mayo Clinic
Conditions:
Pacemaker Insertion
Regional Block
Eligibility:
All Genders
18-100 years
Phase:
NA
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.
Eligibility Criteria
Inclusion
- Age 18-100 years old
- Registered patients at Mayo Clinic in Florida scheduled to undergo primary insertion of pacemaker
Exclusion
- 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
Key Trial Info
Start Date :
November 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2016
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT01473667
Start Date
November 1 2011
End Date
September 1 2016
Last Update
February 1 2019
Active Locations (1)
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1
Mayo Clinic
Jacksonville, Florida, United States, 32224