Trials / Terminated
TerminatedNCT03376256
Compuflo Instrument for Thoracic ES Identification
Evaluation of the Compuflo Epidural Instrument for Thoracic Epidural Space Identification
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 2 (actual)
- Sponsor
- University of Miami · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
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 the thoracic epidural space through measurement of pressure levels. While this device is approved by the FDA for use in the procedure of the lumbar epidural, it is not used to perform the epidural procedure but rather to measure the epidural pressure. This study will likewise measure the epidural pressure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Compuflo Epidural Instrument | Compuflo Epidural Instrument will be used to measure pressure levels in the thoracic epidural space while performing thoracic epidural anesthesia. |
Timeline
- Start date
- 2018-07-11
- Primary completion
- 2018-07-17
- Completion
- 2018-07-17
- First posted
- 2017-12-18
- Last updated
- 2020-12-03
- Results posted
- 2020-12-03
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03376256. Inclusion in this directory is not an endorsement.