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Indiana Spine Group | Carmel, IN

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(Unclaimed)

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ETX-018810
MDT-15
SI-6603

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Active trials

13 of 39 total trials

2-level Cervical Disc Replacement Comparing Prodisc C SK & Vivo to Mobi-C (SMART)

A multi-center, prospective, randomized, controlled comparison of the prodisc C SK and prodisc C Vivo to the control, a similar, legally marketed tot...

Enrolling
Symptomatic Cervical Disc Disease
Device: prodisc C SK and/or Vivo
Device: Mobi-C Cervical Disc

The proposed investigation is a multi-center, prospective, randomized, controlled comparison of the BAGUERA®C to the control, a similar, legally mark...

Active, not recruiting
Cervical Disc Disease
Device: BAGUERA®C Cervical Disc Prosthesis
Device: Mobi-C Cervical Disc

The proposed investigation is a multi-center, prospective, randomized, controlled comparison of the BAGUERA®C to the control, a similar, legally mark...

Active, not recruiting
Cervical Disc Disease
Device: BAGUERA®C Cervical Disc Prosthesis
Device: Mobi-C® Cervical Disc

The purpose of this study is to obtain safety and effectiveness data on the investigational device for multi-level PLF procedures and determine the m...

Active, not recruiting
Multi-Level Degenerative Lumbosacral Spinal Conditions
Device: Infuse Bone Graft
Device: Medtronic DBM

The purpose of this study is to evaluate the safety and efficacy of KUR-113 Bone Graft (TGplPTH1-34 in fibrin) compared to local autograft for the tr...

Active, not recruiting
Degenerative Disc Disease
Spinal Fusion
Other: Autologous Bone Graft
Combination Product: TGplPTH1-34 in fibrin

The LimiFlex™ Clinical Trial is a prospective, concurrently controlled, multi-center study to evaluate the safety and effectiveness of decompression...

Active, not recruiting
Lumbar Spinal Stenosis
Degenerative Spondylolisthesis
Procedure: Decompression
Procedure: Fusion

The aim of this trial is to evaluate if P-15L bone graft (investigational device) is not inferior in effectiveness and safety to local autologous bon...

Active, not recruiting
Degenerative Disc Disease
Device: P-15L Bone Graft
Other: Local autologous bone in a TLIF with Instrumentation

This study is a prospective, randomized study comparing ReActiv8 Therapy to Optimal Medical Management (OMM).

Active, not recruiting
Chronic Low-back Pain
Device: ReActiv8

The purpose of this prospective, single-arm, multicenter study is to assess an annular closure device when used as an adjunct to a primary lumbar lim...

Active, not recruiting
Lumbar Disc Herniation
Device: Annular closure device

The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal in...

Enrolling
Spinal Trauma
Spinal Tumor Case
Device: Follow-up schedule: pre-operative baseline up to 24-months post-procedure
Device: Follow-up schedule: pre-operative baseline to discharge

A multicenter, prospective, non-randomized, historically controlled study. To demonstrate the Synergy Disc is at least as safe and effective as conve...

Active, not recruiting
Cervical Degenerative Disc Disease
Device: Anterior Cervical Discectomy and Fusion

A multicenter, prospective, non-randomized, historically controlled study. Demonstrate the Synergy Disc is at least as safe and effective as conventi...

Active, not recruiting
Cervical Degenerative Disc Disease
Device: Anterior Cervical Discectomy & Fusion

This is a global, multi-center, prospective, randomized, blinded, controlled pivotal study. Clinical and radiological evaluation will be performed pr...

Enrolling
Degenerative Disease of the Lumbosacral Spine
Device: Infuse™ Bone Graft (Infuse™)
Device: Intervertebral body fusion device and Medtronic posterior Fixation Systems

Trial sponsors

Medtronic logo
R
NuVasive logo
B
M
S
S
Abbott logo
B
C

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