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Study identifier: NCT07414745 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

MDT-0123 Japan Study

Condition: Disc Degeneration · Spinal Deformity  ·  Sponsor: Medtronic Spinal and Biologics

PhasePhase 3
Planned participants140
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The purpose of this clinical trial is to compare the efficacy and safety of this investigational device with autologous iliac bone graft (ICBG) in patients who are deemed to require bone fusion through spinal fixation at two levels (ALIF or OLIF) due to disc degeneration or spinal deformity in the lumbosacral spine (L2-S1) for intervertebral support and correction with the aim of stabilizing the spine.

This description comes directly from the study's public registry record.

Talk to the study team

Aki Shiomitsu  ·  +8108070920518  ·  aki.shiomitsu@medtronic.com

Always discuss trial participation with your own doctor first.

Locations (14)

Kobe University HospitalKobe, Hyōgo, JapanRecruiting
Tokai University HospitalIsehara, Kanagawa, JapanNot Yet Recruiting
Wakakusa Daiichi HospitalHigashiosaka, Osaka, JapanNot Yet Recruiting
Dokkyo Medical University Saitama Medical CenterKoshigaya, Saitama, JapanNot Yet Recruiting
Seirei Hamamatsu General HospitalHamamatsu, Shizuoka, JapanNot Yet Recruiting
Sonoda Medical Corporations Sonoda Third HospitalAdachi-Ku, Tokyo, JapanRecruiting
Toranomon HospitalMinato-Ku, Tokyo, JapanNot Yet Recruiting
Tokyo General HospitalNakano-Ku, Tokyo, JapanNot Yet Recruiting
Shunyokai Medical Corporation Sangubashi Spine Surgery HospitalShibuya-Ku, Tokyo, JapanNot Yet Recruiting
Keio University HospitalShinjuku-Ku, Tokyo, JapanNot Yet Recruiting
Kyoto City HospitalKyoto, JapanRecruiting
Kitano Medical Research Institute HospitalOsaka, JapanRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07414745