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Completed
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NCT04061759 -
Physiotherapy in Lumbar Disc Pathologies
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N/A |
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Recruiting
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NCT04727385 -
Intervertebral DXM Gel Injection in Adults With Painful Lumbar Degenerative Disc Disease
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N/A |
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Completed
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NCT04587401 -
The Effects of Anesthesia on Cerebral Perfusion in Patients With High Blood Pressure
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N/A |
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Not yet recruiting
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NCT06034041 -
The Effect of Mediclore as an Anti-adhesion Agent and Safety in Full-endoscopic Spine Surgery: a Preliminary Study
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Phase 4 |
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Recruiting
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NCT04134975 -
Evaluation of the Contribution of Intraoperative Scans Coupled With the Navigation for the Precision of the Positioning of the Pedicle Screws During a Lumbar Spine Surgery: a Prospective Randomised Study
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N/A |
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Recruiting
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NCT05146583 -
Injection of Autologous Bone Marrow Aspirate in Patients With Degenerative Disc Disease.
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|
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Recruiting
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NCT04641039 -
Postoperative Scar in the Control Excess of Mobility Induced by Annulus Removal on Inserting a Lumbar Disc Prosthesis
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N/A |
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Completed
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NCT04301232 -
Fast-Track Eligibility and Hospital Discharge for Outpatient Lumbar Discectomy
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|
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Recruiting
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NCT06154005 -
OsteoAdapt SP Advanced Bone Graft Feasibility Study - Transforaminal Interbody Lumbar Fusion
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Phase 1/Phase 2 |
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Completed
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NCT03977961 -
The Six-Minute Walking Test (6MWT) as a Measure of Functional Impairment in Lumbar Degenerate Disc Disease.
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|
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Enrolling by invitation
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NCT05444751 -
GA + ESP vs. SA + ESP in Lumbar Decompression Surgeries
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Phase 3 |
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Completed
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NCT02700451 -
Post-op Acetaminophen vs NSAID Use on Lumbar Spinal Fusion Outcomes
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N/A |
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Completed
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NCT02421601 -
A Study of SI-6603 in Patients With Lumbar Disc Herniation
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Phase 3 |
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Active, not recruiting
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NCT03733626 -
Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease
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N/A |
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Recruiting
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NCT04042844 -
A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)
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Phase 2 |
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Recruiting
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NCT06462729 -
LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF)
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Phase 1/Phase 2 |
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Completed
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NCT05345249 -
Erector Spinae Plane Block as Pain Management After Lumbar Fusion Surgery
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Phase 4 |
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Active, not recruiting
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NCT03060434 -
Pentoxifylline and Lumbar Radiculopathy
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Phase 4 |
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Withdrawn
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NCT02852187 -
Single Center Study Comparing MOBIS II ST vs MOBIS PEEK
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N/A |
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Completed
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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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