Clinical Trials Sponsored by SpineX Inc.

Total 35829 results

SpineX Inc.

Not yet recruiting

Spinal Cord Innovation in Pediatrics (SCiP) to Treat SensoriMotor Function in Children Cerebral Palsy: Protocol for a Randomized Controlled Trial

Cerebral Palsy
SpineX Inc.

Recruiting

Noninvasive Spinal Neuromodulation Enables Locomotor Recovery in Individuals With Cerebral Palsy

Cerebral Palsy

United States
Alphatec Spine, Inc.

Terminated

OsseoFix™ Spinal Fracture Reduction System in Treating Spinal Compression Fracture (OsseoFix)

Vertebral Compression Fractures

United States
Alphatec Spine, Inc.

Terminated

PureGen: Radiographic Analysis of Fusion for ACDF

Cervical Degenerative Disc Disease

United States
Interventional Spine, Inc.

Unknown

The PerX360º System™ Registry (OptiLIF™)

DDD

United States
Interventional Spine, Inc.

Terminated

Percutaneous Dynamic Stabilization (PDS) System Versus Fusion for Treating Degenerative Disc Disease

Lumbar Degenerative Disc Disease

United States
Alphatec Spine, Inc.

Recruiting

Intraoperative Monitoring for the Lateral Lumbar Interbody Fusion Procedure

Intervertebral Disc Degeneration | Spondylolisthesis | Spinal Deformity | Stenosis, Spinal | Spinal Instability

United States
Interventional Spine, Inc.

Withdrawn

A Post-Market Study of Transfacet Lumbar Spine Fixation and Fusion Utilizing the PERPOS™ PLS System

Lumbar Facet Disease
Alphatec Spine, Inc.

Terminated

Radiographic Analysis Using PureGen Versus Autologous Bone in Posterolateral Fusion (PLF)

Lumbar Degenerative Disc Disease

United States
Alphatec Spine, Inc.

Completed

OsseoScrew Versus Fenestrated Pedicle Screws Augmented With Polymethylmethacrylate (EVOLVE)

Osteoporosis | Poor Bone Quality

Belgium, Spain, Germany, Italy, United Kingdom
Alphatec Spine, Inc.

Terminated

Radiographic and Clinical Outcomes of PureGen in Posterior Lumbar (PLIF) and Transforaminal Interbody Fusion (TLIF)

Lumbar Degenerative Disc Disease

United States
Medtronic Spine LLC

Completed

FREE Study - Fracture Reduction Evaluation

Multiple Myeloma | Bone Neoplasms | Osteoporosis | Osteopenia

United States
Medtronic Spine LLC

Completed

Long-Term Outcomes for Lumbar Spinal Stenosis Patients Treated With X STOP®

Lumbar Spinal Stenosis

United States
Medtronic Spine LLC

Completed

CAFE Study - Cancer Patient Fracture Evaluation (CAFE)

Cancer | Spinal Fractures

United States, Canada, Australia, Sweden, Belgium, Germany, Hungary, United Kingdom
Medtronic Spine LLC

Withdrawn

Effects of X-STOP® Versus Laminectomy Study (EXELS)

Lumbar Spinal Stenosis
Medtronic Spine LLC

Completed

Medtronic SCORE Study - Study of Curette Use for Obtaining Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty (MDTSCORE)

Vertebral Body Compression Fractures (VCFs)

Germany, United States, Belgium
Spirox, Inc.

Completed

Evaluation of an Absorbable Implant for the Treatment of Nasal Valve Collapse

Nasal Valve Collapse

Germany
Spirox, Inc.

Completed

Spirox Latera™ Implant Support of Lateral Nasal Wall Cartilage (LATERAL-OR) Study

Nasal Obstruction

United States
Medtronic Spine LLC

Completed

Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back Pain (SODA)

Low Back Pain

United States
Medtronic Spine LLC

Terminated

KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restoration of Vertebral Body Compression Fractures

Vertebral Body Compression Fractures

United States, Canada
Medtronic Spine LLC

Terminated

Condition of Approval Study (COAST)

Lumbar Spinal Stenosis

United States
Spine BioPharma, Inc
MCRA

Recruiting

Moderate - Severe Degenerative Disc Disease Evaluation of the Lumbar Spine (MODEL)

Lumbar Degenerative Disc Disease

United States
K2M, Inc.
Stryker Spine

Withdrawn

Clinical and Radiographic Outcomes of Spine Surgeries Utilizing Capri Cervical and Thoracolumbar Corpectomy Cage Systems

Cervical Spine Injury | Thoracolumbar Spine
Scilex Pharmaceuticals, Inc.

Completed

Study to Evaluate the Safety of SP-104

Healthy Volunteers

New Zealand
Scilex Pharmaceuticals, Inc.

Completed

Pharmacokinetics and Adhesion of Lidocaine Topical System 1.8% With Water Exposure

Healthy

United States
Spinal Restoration, Inc.

Completed

Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® Disc Augmentation System: A Pilot Study

Low Back Pain

United States
Spire, Inc.

Completed

Spire Medical Health Tag Actigraphy and Sleep Validation in Adults

Healthy Volunteers

United States
Scilex Pharmaceuticals, Inc.

Completed

Pharmacokinetics of SP-104

Healthy

New Zealand
Scilex Pharmaceuticals, Inc.

Completed

Clinical Adhesion Study Between ZTlido 1.8% and Three Over-the-counter External Analgesic Lidocaine-containing Patches

Healthy

United States
Scilex Pharmaceuticals, Inc.

Completed

Comparative Pharmacokinetic Study of Lidocaine Patch 1.8% (ZTlido™) and Lidocaine Patch 5% (Lidoderm®) in Healthy Subjects

Healthy
Scilex Pharmaceuticals, Inc.

Completed

Pharmacokinetics and Adhesion of Lidocaine Topical System 1.8% Under Conditions of Heat and Exercise

Healthy
Spinal Restoration, Inc.

Terminated

Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® System

Back Pain | Degenerative Disc Disease | Chronic Low Back Pain | Internal Disc Disruption

United States
Aminex Therapeutics, Inc.

Recruiting

Oral AMXT 1501 Dicaprate in Combination With IV DFMO

Melanoma | Cervical Cancer | Cancer | Breast Cancer | Head and Neck Cancer | Gastric Cancer | Colorectal Cancer | Esophageal Cancer | Solid Tumor | Endometrial Cancer | Advanced Cancer | Diffuse Midline Glioma, H3 K27M-Mutant | Papillary Thyroid Cancer | Solid Carcinoma | Mesotheliomas Pleural | Glioma, Malignant | Ovary Cancer and other conditions

United States, Australia
Scilex Pharmaceuticals, Inc.

Completed

Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Generic Lidocaine Patch 5% in Healthy, Adult, Human Subjects

Healthy

United States
Aminex Therapeutics, Inc.

Completed

Oral AMXT 1501 Dicaprate in Combination With DFMO

Cancer | Solid Tumor | Advanced Cancer | Solid Carcinoma

United States
Scilex Pharmaceuticals, Inc.

Completed

Pharmacokinetic Study of SP-103 in Healthy Adult Human Subjects

Healthy

United States
Scilex Pharmaceuticals, Inc.

Completed

Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Lidocaine Patch 5% and Lidocaine Medicated Plaster 5% in Healthy, Adult, Human Subjects

Healthy

United States
Scilex Pharmaceuticals, Inc.

Completed

Adhesion of Lidocaine Topical System 1.8%

Healthy
Scilex Pharmaceuticals, Inc.

Completed

Pharmacokinetic Study of Lidocaine Patch 1.8% Lidocaine Patch 5% (Lidoderm®) in Healthy Subjects

Healthy
John Papakonstantinou, MD
Scilex Ltd.

Completed

Lidocaine Patch 1.8% for Moderate to Severe Pain From Carpal Tunnel Syndrome (CTS)

Carpal Tunnel Syndrome

United States
Sinew Pharma Inc.

Completed

Phase I Pharmacokinetic Study of HUYPS-1 in Healthy Volunteers

Nonalcoholic Steatohepatitis

Taiwan
Sinew Pharma Inc.

Terminated

An Open-Label Study to Assess the Hepatic Protection Effect of SNP-612, in Patients With NAFLD

NASH - Nonalcoholic Steatohepatitis

Taiwan
Apnex Medical, Inc.

Completed

Australian Clinical Study of the Apnex Medical HGNS System to Treat Obstructive Sleep Apnea

Obstructive Sleep Apnea
Sonex Health, Inc.

Recruiting

Post-Market Registry of the Patient Experience When Using UltraGuideCTR for Carpal Tunnel Release (MISSION)

Carpal Tunnel Syndrome | CTS

United States
Sinew Pharma Inc.

Not yet recruiting

A Randomized, Double-Blind, Placebo Controlled Study to Assess the Efficacy and Safety of SNP-610 for the Treatment of Patients With Non-alcoholic Steatohepatitis

NASH - Nonalcoholic Steatohepatitis
Sonex Health, Inc.

Completed

Trial of Ultrasound Guided Carpal Tunnel Release Versus Traditional Open Release (TUTOR) (TUTOR)

Carpal Tunnel Syndrome | CTS | Carpal Tunnel

United States
Sinew Pharma Inc.

Completed

A Randomized, Single-blind, Parallel Group and Multiple - Dose Design Study

Acetaminophen Toxicity

Taiwan
Sinew Pharma Inc.

Completed

A Phase I Study to Investigate the Safety, Tolerability and Pharmacokinetic Profile of SNP-630 in Health Subjects.

NASH - Nonalcoholic Steatohepatitis

Taiwan
Apnex Medical, Inc.

Terminated

Apnex Clinical Study of the Hypoglossal Nerve Stimulation (HGNS®) System to Treat Obstructive Sleep Apnea

Obstructive Sleep Apnea

United States, Australia
Sinew Pharma Inc.

Recruiting

A Partial Randomized, Single-blind or Open-label, Dose-escalation With Multiple-dose Design Study to Evaluate the Pharmacokinetics of Acetaminophen and Its Toxic Metabolites With Panadol® and SafeTynadol® in Healthy Volunteers

Hepatitis | Pharmacology

Taiwan

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