OLIF25™ /OLIF51™ Study

Medtronic

Status: Terminated

Conditions: Degenerative Disc Disease; Scoliosis

Treatments: Procedure: Oblique Lateral Interbody Fusion

Study type: Observational

Funder types: Industry

Identifiers

NCT02657421

P15-05

Details and patient eligibility

About

The purpose of this single-arm observational study is to observe and document clinical outcomes of the OLIF25™ and OLIF51™ procedures in patients diagnosed with degenerative disc disease or degenerative scoliosis, and report the rate of adverse events of interest through the 24 months follow-up visit.

Enrollment: 168 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patient is 18 years of age or older.
2. Patient agrees to participate in the study and is able to sign the informed consent/data release form.
3. Patient is undergoing surgery from L2-L5 for OLIF25™ and/or from L5-S1 for OLIF51™ for degenerative disc disease or degenerative scoliosis.

Exclusion criteria

1. Illiterate or vulnerable patients (e.g. minors, participants incapable of judgment).