OLIF25™ /OLIF51™ Study



Status:Terminated
Conditions:Orthopedic, Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:6/6/2018
Start Date:November 2015
End Date:May 3, 2018

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A Multi-Center, Prospective, Observational Study to Assess Outcomes for Patients Treated for Lumbar Spinal Conditions Using an OLIF25™ and/or OLIF51™Approach

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.


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).
We found this trial at
7
sites
205 East NASA Boulevard #200
Melbourne, Florida
Principal Investigator: Richard Hynes, MD
Phone: 321-541-1587
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206 De Frélaan
Brussels, 1180
Principal Investigator: Philip Leijssen, MD
Phone: +322 614 2720
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Brussels,
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Murrieta, California 92563
Principal Investigator: Kamal Woods, MD
Phone: 707-694-2372
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Murrieta, CA
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165 West 86th Street
New York, New York 10034
Principal Investigator: Ronald Lehman, MD
Phone: 212-932-4410
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New York, NY
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Pittsburgh, Pennsylvania 15212
Principal Investigator: Michael Oh, MD
Phone: 412-359-4272
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Pittsburgh, PA
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500 Parnassus Ave
San Francisco, California 94143
(415) 476-9000
Principal Investigator: Dean Chou, MD
Phone: 415-353-2240
University of California at San Francisco (UCSF) The leading university exclusively focused on health, UC...
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Tampa, Florida 33637
Principal Investigator: Jim Billys, MD
Phone: 813-978-9700
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Tampa, FL
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