REFINE Study: A Study In a Novel Interspinous Fusion Device In Subjects With Low Back Pain

NARecruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

March 19, 2021

Primary Completion Date

January 1, 2028

Study Completion Date

January 1, 2028

Conditions
Lumbar Spinal Stenosis
Interventions
DEVICE

Interspinous Fusion

The intended study population are adults 18 years or older with symptomatic lumbar degenerative disc disease resulting in back pain with lower extremity symptoms and neurogenic claudication that improves with spinal flexion who are candidates for use of the Zip™ MIS Interspinous Fusion device when undergoing spinal fixation procedures.

Trial Locations (10)

17601

RECRUITING

Center for Interventional Pain and Spine, Chadds Ford

20745

RECRUITING

National Spine and Pain Centers, Oxon Hill

RECRUITING

Nevada Advanced Pain Specialists, Reno

33477

RECRUITING

The Raso Pain Center, Jupiter

45140

RECRUITING

Premier Pain Treatment Institute, Loveland

70458

RECRUITING

Koga Neurosurgery, Slidell

89509

RECRUITING

Comprehensive & Interventional Pain Management, Henderson

RECRUITING

Reno Tahoe Pain Associates, Reno

95403

ACTIVE_NOT_RECRUITING

Evolve Restorative Center, Santa Rosa

08043

RECRUITING

The Pain Management Center, Voorhees Township

Sponsors
All Listed Sponsors
lead

Pacific Research Institute

NETWORK

NCT05504499 - REFINE Study: A Study In a Novel Interspinous Fusion Device In Subjects With Low Back Pain | Biotech Hunter | Biotech Hunter