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OLIF25™ /OLIF51™ Study

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Medtronic

Status

Terminated

Conditions

Degenerative Disc Disease
Scoliosis

Treatments

Procedure: Oblique Lateral Interbody Fusion

Study type

Observational

Funder types

Industry

Identifiers

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).

Trial contacts and locations

12

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Data sourced from clinicaltrials.gov

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