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Clinical Trial Summary

The aim of this study is to demonstrate the feasibility of a new technique using real time ultrasound guided paramedian approach to the epidural space. This approach will use transverse view of the spine utilizing curvilinear low frequency ultrasound probe "Sonosite S nerve" and echogenic 17G tuohy needles " Pajunk TuohySono"

The investigators believe that this new technique is helpful to get the best anatomic landmark for epidural catheter placement using the real-time ultrasound.

Measurable outcomes:

- Block performance time.

- Block success rate.

- Needle Depth to epidural space

Block success rate will be measured as the rate of cases that will have successful insertion of the epidural catheter using ultrasound guidance and the case is done completely under epidural anesthesia.

All cases that will be converted to general anesthesia will be counted unsuccessful.

Other measurable outcome data that will be collected will include needle depth to the epidural space, and ultrasound measured depth to the lamina


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01686243
Study type Interventional
Source The Cleveland Clinic
Contact
Status Completed
Phase N/A
Start date July 2012
Completion date November 25, 2016

See also
  Status Clinical Trial Phase
Not yet recruiting NCT06460155 - CompuFlo CathCheck Phase 4
Withdrawn NCT03378492 - Utilizing Ultrasound for Residents as an Aid in Epidural Placement N/A
Completed NCT05616299 - BrightPoint Reflectometer Device Study N/A