N/A N=286 A Multicenter Prospective Study of Quality of Life in Adult Scoliosis
Scoliosis
Primary: Scoliosis Research Society Quality of Life Questionnaire (SRS QOL) Subscore — 0.5; 0.5 score on a scale — p=<0.001
Clinical Trial Search
Completed trials with posted results — search by concept, filter by the parameters that matter at the bedside.
N/A N=178 Lumbar Degenerative Disc Disease Treated With Anterior Tension Band System (ATB) With ALIF/FRA Spacer
Lumbar Degenerative Disc Disease
Primary: Number of Subjects With Successful Radiographic Fusion — 90 Participants
N/A N=71 Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric Neuromuscular Spinal Deformity
Neuromuscular Diseases · Neuromuscular Scoliosis
Primary: First Scoliotic Curve — 71.4029 degrees
N/A N=20 Vertebral Body Tethering Outcomes for Pediatric Idiopathic Scoliosis
Idiopathic Scoliosis
Primary: Incidence of Treatment-Emergent Adverse Events — 11; 7; 20; 0 Participants
N/A N=58 Pedicle Screw Usage in Conventional Fixation Pattern Constructs Compared to Thoracic Hook Constructs in Scoliosis
Adolescent Idiopathic Scoliosis
Primary: Main Thoracic Cobb — 55; 58; 15; 18 Degree
N/A N=337 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Degenerative Lumbar Spine (MASTERS-D2)
Intervertebral Disc Degeneration
Primary: Change (Preop-postop) of Disability, Oswestry Disability Index (ODI) at 3 Months as Compared to Baseline in DDD Patients With Spondylolisthesis — 23.19; 26.08 change of…
N/A N=100 Sagittal Plane Shear Index for Planning Lumbar Stenosis Surgery
Lumbar Spinal Stenosis · Spondylolisthesis
Primary: Proportion of Surgical Plans Recorded Prior to the SPSI Report That Are Altered After Integration of SPSI Into the Surgical Planning — 47; 22; 6 Surgical plans
Phase 4 N=146 Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treatment of Complex Disc Disease
Sciatica · Back Pain
Primary: To Demonstrate a Statistically Significant Difference in the Relief of Back Pain Between Both Treatment Groups. The Endpoint Will be the Difference Between Baseline and…
N/A N=252 A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal Technologies) Fusion Procedures for the Treatment of the Degenerative Lumbar Spine
Degenerative Lumbar Spine Causing Back and/or Leg Pain · Lumbar Spine Degeneration
Primary: Time From Surgery to First Ambulation. — 1.3 Days from surgery to first ambulation
N/A N=20 Clinical and Radiological Evaluation of Patients With DDD Following TLIF With 3-D Printed Titanium Cage
Intervertebral Disc Disease
Primary: Fusion Rate — 19; 1; 0 Participants
N/A N=64 Evaluation of 3D Machine-vision Image Guided Surgery Spine Navigation
Spinal Stenosis, Lumbar Region · Spondylolisthesis
Primary: Mean Total Length of Operative Time — 218; 218.5 minutes
N/A N=24 Erector Spinae Plane Blocks for Adolescent Idiopathic Scoliosis
Pain, Postoperative · Opioid Use · Recruitment
Primary: Number of Patients Who Receive Bilateral, Pre-incision ESPB — 9; 12 Participants
Phase 3 N=52 Tranexamic Acid Dosing in Adult Spinal Deformity Surgery
Adult Spinal Deformity
Primary: Blood Loss — 2046; 1596 mL
N/A N=231 Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease
Degenerative Disc Disease
Primary: Radiographic Fusion — 66; 46; 37; 75 percentage of subjects
N/A N=184 Understanding Non-Response in Spine Fusion Surgery
Spine Fusion
Primary: Oswestry Disability Index — 41.3; 30.4; 19.4 score on a scale
N/A N=66 Use of Ultrasonic Bone Scalpel in Adolescent Idiopathic Scoliosis
Adolescent Idiopathic Scoliosis · Posterior Spinal Fusion
Primary: Estimated Blood Loss/Level — 35.21; 38.68 mL
Phase 4 N=55 MiDAS II (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation Study
Lumbar Spinal Stenosis
Primary: Changes in Back Pain as Measured by a 10-point Visual Analog Scale (VAS). — 3.59 units on a scale — p=<0.0001
N/A N=36 Accell Evo3™ Demineralized Bone Matrix in Instrumented Lumbar Spine Fusion
Degenerative Changes · Stenosis · Spondylosis
Primary: Time to Arthrodesis (Fusion) for Each Spinal Level (Unit), as Measured by X-rays. — 6 months to fusion
N/A N=40 Adolescent Idiopathic Scoliosis (AIS) Patient Positioning in EOS System®
Adolescent Idiopathic Scoliosis
Primary: Impact of the Patients' Arm Positioning on Clinical Evaluation of Bi-planar Spinal X-rays Using the EOS System - Spinal Sagittal Plane Parameters — 5.9; 7.6; 29.5; 33.55…
N/A N=72 Minimal Access Surgical Technique (MAST) in Obese Patients in Degenerative Lumbar Disease
Degenerative Lumbar Disease
Primary: Postoperative Complications in the BMI Groups During Post Operative Hospitalization. — 8; 9; 20 Events during hospitalization
N/A N=267 Investigation of the Simplify® Cervical Artificial Disc
Cervical Degenerative Disc Disease
Primary: Number of Participants With Composite Clinical Success (CCS) of Simplify Disc — 68; 132 Participants — p=<.001
Phase 4 N=78 MiDAS I (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation Study
Lumbar Spinal Stenosis
Primary: Mean Change in Back Pain as Measured by a 10-point Visual Analog Scale (VAS). — 3.21 units on a scale — p=<0.0001
N/A N=70 A Prospective Randomized Study on the Clinical Benefits of OrthoPAT Drains
Spine Deformity
Primary: Volume of Allogenic Blood Transfused Postoperatively — 458.33; 382.35 mL
N/A N=500 Comparison of DISCOVER™ Artificial Cervical Disc and ACDF for Treatment of Cervical DDD (IDE Study)
Cervical Degenerative Disc Disease
Primary: Overall Success — 137; 110; 28; 13 participants who are successes
Phase 4 N=162 Intermittent Neurogenic Claudication Treatment With APERIUS®
Spinal Stenosis
Primary: Mean Percentage Change in Symptom Severity at 6 Weeks Compared to Baseline, Using the Patient Completed Zurich Claudication Questionnaire for Symptom Severity — -29.7…
N/A N=119 MaxAn Post Market Surveillance Validation
DDD · Deformity · Tumor
Primary: Number of Participants With Differing Severity of Adjacent Level Ossification — 36; 38; 16; 10 Participants
N/A N=376 Activ-L™ Artificial Disc Treatment of Degenerative Disc Disease in the Treatment of Degenerative Disc Disease
Degenerative Disc Disease
Primary: Overall Success at 24 Months Relative to Baseline — 42.2; 28.3; 61.9; 52.8 percentage of participants — p=<0.05
N/A N=1,674 Postmarket Registry for Evaluation of the Superion® Spacer
Lumbar Spinal Stenosis
Primary: Vertiflex® Patient Satisfaction Survey — 1147 Participants
N/A N=118 ViBone in Cervical and Lumbar Spine Fusion
Spondylosis · Cervical Spondylosis · Spondylolisthesis
Primary: Fusion Rates Per Level Using the Bridwell Interbody Grading Scale — 64; 50 Fusions
N/A N=3 Spinal Cord Stimulation in Spinal Muscular Atrophy
Spinal Muscular Atrophy Type 3 · Spinal Muscular Atrophy Type 4
Primary: Muscle Weakness — 2; 3 Participants