Lumbar Disc Disease Clinical Trial
Official title:
A Multicenter, Open-label Study of SI 6603 in Patients With Lumbar Disc Herniation (Phase III)
The purpose of this study is to evaluate the safety and efficacy of SI-6603(Condoliase) in patients with lumbar disc herniation.
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Status | Clinical Trial | Phase | |
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Completed |
NCT01941563 -
A Study of SI-6603 in Patients With Lumbar Disc Herniation
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Phase 3 | |
Completed |
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Physiotherapy in Lumbar Disc Pathologies
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N/A | |
Recruiting |
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N/A | |
Completed |
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N/A | |
Recruiting |
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Injection of Autologous Bone Marrow Aspirate in Patients With Degenerative Disc Disease.
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Recruiting |
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Postoperative Scar in the Control Excess of Mobility Induced by Annulus Removal on Inserting a Lumbar Disc Prosthesis
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N/A | |
Completed |
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Fast-Track Eligibility and Hospital Discharge for Outpatient Lumbar Discectomy
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Recruiting |
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OsteoAdapt SP Advanced Bone Graft Feasibility Study - Transforaminal Interbody Lumbar Fusion
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Phase 1/Phase 2 | |
Completed |
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The Six-Minute Walking Test (6MWT) as a Measure of Functional Impairment in Lumbar Degenerate Disc Disease.
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Enrolling by invitation |
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GA + ESP vs. SA + ESP in Lumbar Decompression Surgeries
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Phase 3 | |
Completed |
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Post-op Acetaminophen vs NSAID Use on Lumbar Spinal Fusion Outcomes
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N/A | |
Active, not recruiting |
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Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease
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N/A | |
Recruiting |
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A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)
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Phase 2 | |
Recruiting |
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LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF)
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Phase 1/Phase 2 | |
Completed |
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Erector Spinae Plane Block as Pain Management After Lumbar Fusion Surgery
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Phase 4 | |
Active, not recruiting |
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Phase 4 | |
Withdrawn |
NCT02852187 -
Single Center Study Comparing MOBIS II ST vs MOBIS PEEK
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N/A | |
Completed |
NCT04062942 -
The Six-Minute Walking Test (6WT) and Timed-Up-and-Go (TUG) Test as Measures of Objective Functional Impairment in Patients Undergoing Interlaminar or Transforaminal Epidural Steroid Injection for Lumbar Degenerative Disc Disease (DDD)
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