Trials / Terminated
TerminatedNCT01473667
Superficial Cervical Plexus Block for Pacemaker Insertion
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Mayo Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Superficial Cervical Plexus Block (SCP) block | SCP block using 10-15ml of 1% Ropivacaine |
| PROCEDURE | Local site infiltration | Local site infiltration using 2% lidocaine |
Timeline
- Start date
- 2011-11-01
- Primary completion
- 2015-03-01
- Completion
- 2016-09-01
- First posted
- 2011-11-17
- Last updated
- 2019-02-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01473667. Inclusion in this directory is not an endorsement.