NCT02378727 - CompuFlo® Assessment Study for the Epidural Space Verification | Biotech Hunter

Enrollment

400

Participants

Timeline

Start Date

January 31, 2015

Primary Completion Date

July 31, 2016

Study Completion Date

July 31, 2016

Conditions

Verification of Needle Tip Placement in the Lumbar Epidural Space

Interventions

DEVICE

Active: Comparator Loss Of Resistance Syringe

Lumbar epidural procedure utilizing Loss of Resistance Syringe

DEVICE

Experimental: CompuFlo® Epidural System

CompuFlo® Epidural is intended for use with an epidural needle for the verification of needle tip placement in the lumbar epidural space

Trial Locations (5)

Northwestern Memorial Hospital, Chicago

University of Texas Houston, Houston

San Diego Pain Institute, San Diego

Vitamed Research, Rancho Mirage

University of California Irvine, Irvine