Status:
TERMINATED
Compuflo Instrument for Thoracic ES Identification
Lead Sponsor:
University of Miami
Conditions:
Anesthesia
Thoracic
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The purpose of this pilot study is to evaluate whether the Compuflo Epidural Instrument injection pump technology, which is FDA approved for lumbar epidural anesthesia, is also capable of identifying ...
Eligibility Criteria
Inclusion
- Age 18 to 80 years inclusive
- BMI 18.5 to 40 inclusive
- Scheduled for thoracic epidural anesthesia
Exclusion
- Patients younger than 18 years or older than 80 years of age
- Patients with BMI less than 18.5 or greater than 40
- Contraindication to thoracic epidural anesthesia
- Allergy or hypersensitivity to local anesthetics
- Patients with preexisting nerve damage
- Patients unable to provide written informed consent
- Individuals of vulnerable populations: children, pregnant women, prisoners
Key Trial Info
Start Date :
July 11 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 17 2018
Estimated Enrollment :
2 Patients enrolled
Trial Details
Trial ID
NCT03376256
Start Date
July 11 2018
End Date
July 17 2018
Last Update
December 3 2020
Active Locations (1)
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1
University of Miami Hospital
Miami, Florida, United States, 33136