35
Participants
Start Date
June 28, 2024
Primary Completion Date
December 31, 2027
Study Completion Date
December 31, 2027
CONDUIT
Arm Description: Group/Cohort Description: This cohort is composed of patients who will be prospectively enrolled (35 total). These patients will undergo spinal stabilisation for lumbar degenerative disease using the CONDUIT ALIF cage system with supplemental posterior fixation. This device is FDA approved thus this is post market observational intervention.
RECRUITING
Mater Misericordiae University Hospital, Dublin
Mater Misericordiae University Hospital
OTHER
University College Dublin
OTHER