NCT01316211 - Clinical Trial Comparing Decompression With and Without Coflex™ Interlaminar Technology Treating Lumbar Spinal Stenosis | Biotech Hunter

Enrollment

246

Participants

Timeline

Start Date

January 31, 2008

Primary Completion Date

August 31, 2014

Study Completion Date

August 31, 2014

Conditions

Spinal Stenosis

Interventions

DEVICE

Implantation of coflex™ after surgical decompression

The device will be implanted after surgical decompression in patients with spinal stenosis.

PROCEDURE

Surgical decompression

Surgical decompression in patients with spinal stenosis without stabilization by an additional implant

Trial Locations (8)

Oberlinklinik Potsdam Orthopädische Fachklinik, Potsdam

Chirurgische Universitätsklinik Rostock Neurochirurgie, Rostock

Klinik für Neurochirurgie Lübeck, Lübeck

Klinik für Wirbelsäulenchirurgie mit Skoliosezentrum Klinikum Neustadt, Neustadt

Ostseeklinik Damp Neurochirurgie, Damp

Otto-von-Guericke-Universität Magdeburg Klinik für Orthopädie, Magdeburg

Orthopädische Universitätsklinik Frankfurt a.M., Frankfurt a.M.

Klinikum Ingolstadt Neurochirurgie, Ingolstadt