Search clinical trials for: Core decompression/PREOB® implantation

Total 630 results

Cantonal Hospital of St. Gallen

Terminated

Prevention of Incisional Hernia After Elective Open Abdominal Aortic Aneurysm (AAA) Repair

Abdominal Aortic Aneurysm

Switzerland
BSN Medical GmbH

Completed

Study to Evaluate Made-to-measure Compression Garments

Lymphedema

Germany
ArthroCare Corporation

Completed

Plasma Disc Decompression Versus Conservative Care

Decompression, Surgical

Finland, Sweden, United Kingdom
MiMedx Group, Inc.

Completed

Amniotic Membrane in Decompressive Craniectomy to Reduce Scarring

Scarring

United States
Ohio State University
Neuright, Inc.

Not yet recruiting

Spinal Cord Stimulation and Small Fiber Peripheral Neuropathy

Diabetic Peripheral Neuropathy

United States
Nij Smellinghe Hosptial

Completed

Comparison Between a Non-elastic Falcro Device and Current Method After Total Knee Arthroplasty

Lymphedema

Netherlands
Le Club Mousse

Completed

Efficacy on Pain Following a Procedure for Injecting Sclerotherapeutic Foam Into the Great Saphenous Vein

Venous Disease
Neuralstem Inc.

Unknown

Dose Escalation and Safety Study of Human Spinal Cord Derived Neural Stem Cell Transplantation for the Treatment of Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis

United States
Eye-yon Medical

Active, not recruiting

EndoArt® Implantation in Subjects With Chronic Corneal Edema

Corneal Edema

Israel, Georgia, Germany, India, France, Netherlands
R3 Vascular Inc.
Cardiovascular Research Foundation, New York; Massachusetts General Physicians...

Recruiting

Study of the R3 Vascular Drug-Eluting Bioresorbable Scaffold in Treating Below the Knee Arterial Disease (RESOLV I)

Peripheral Arterial Disease | Lower Extremity Claudication | Lower Extremity Ischemia | Atherosclerotic Lesion

Canada, Italy, Austria
Medtronic Cardiovascular

Completed

Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in Very High Risk Subjects and High Risk Subjects Who Need Aortic Valve Replacement

Severe Aortic Stenosis

United States
Medtronic Cardiovascular

Active, not recruiting

Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Severe, Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI). (SURTAVI)

Severe Aortic Stenosis

United States, Netherlands, Canada, Spain, Denmark, United Kingdom, Switzerland, Germany, Sweden
Tissue Tech Inc.

Completed

Non-healing Diabetic Foot Ulcers (DFU) Treated With SoC With or Without NEOX®CORD 1K

Diabetic Foot Ulcers

United States, Canada
Medtronic Cardiovascular

Active, not recruiting

Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptomatic Severe Aortic Stenosis With Significant Comorbidities in Extreme Risk Subjects Who Need Aortic Valve Replacement

Severe Aortic Stenosis

United States
Symatese

Unknown

Evaluation of NEVELIA® in Terms of Safety and Efficacy for Third-degree Burns Treatment or Reconstructive Surgery (NEVAL)

Third-degree Burns | Reconstructive Surgery

France
Thuasne
University Hospital, Tours; Delta Consultants

Completed

Physiological Study to Assess Mechanism of Action of MOBIDERM® in Lower-limb Lymphedema Patients (ACTIODERM)

Lymphedema, Secondary | Lymphedema of Leg | Lymphedema Congenital | Lymphedema Primary

France
Samir Saba
Abbott

Recruiting

Arrhythmia Detection After MI (AID MI)

Acute Myocardial Infarction

United States
Hebei Medical University

Recruiting

Application and Research of Mesenchymal Stem Cells in Alleviating Severe Development of COVID-19 Infection

COVID-19

China
Hamad Medical Corporation

Completed

Hyperbaric Oxygen Therapy Versus Core Decompression Augmented With Bone Substitute in Pre Collapse of Avascular Necrosis of Femoral Head

AVN

Qatar
University of Texas Southwestern Medical Center

Recruiting

Comprehensive Optimization At-time of Radical Cystectomy Intervention (COARC)

Bladder Cancer | Radical Cystectomy

United States
University of Alberta
Cross Cancer Institute

Active, not recruiting

Decongestive Exercise and Compression for Breast Cancer Related Lymphedema Management (DREAM)

Lymphedema | Breast Neoplasm

Canada
University Hospital, Caen

Recruiting

Diagnostic Performance of General Practitioners in Compression UltraSound (GPCUS)

Deep Vein Thrombosis

France
Nurami Medical Ltd

Completed

A Prospective, Randomized, Controlled Multi-center Study of ArtiFascia® Dural Repair Patch Compared With Commercially Available Dural Substitutes. To Evaluate the Safety and Effectiveness of ArtiFascia® in Subjects Requiring Dural Repair. (NEOART)

Cerebrospinal Fluid Leak | Dural Tear

Spain, Belgium, Poland, Czechia, Israel
University Hospital, Basel, Switzerland

Completed

Kinesiotape Treatment for Postoperative Edema After Joint Replacement Surgery of the Knee- The KNEETAPE Study (KNEETAPE)

Postoperative Edema

Switzerland
Bone Therapeutics S.A

Completed

Phase 1/2a Study on Allogeneic Osteoblastic Cells Implantation in Delayed-Union Fractures

Long Bone Delayed-Union Fracture
Centre Hospitalier Universitaire de Nīmes

Withdrawn

Effect of Pneumatic Intermittent Venous Compression on Fluid Volumes Infused During Major Abdominal Surgery

Major Abdominal Surgery

France
University Hospital Inselspital, Berne

Completed

Feasibility and Comparison of Continuously Monitored Vital Signs in Pediatric Patients With Cancer.

Febrile Neutropenia | Pediatric Cancer | Oncology | Chemotherapy-induced Neutropenia

Switzerland
Colchester Hospital University NHS Foundation Trust

Completed

Juxta-CuresTM Versus Bandaging for Venous Ulcers (Juxta-Cures)

Venous Ulcer

United Kingdom
Western Vascular Institute, Ireland

Completed

Negative Pressure Vs. Compression in Venous Ulcers

Varicose Ulcer

Ireland
Biosolution Co., Ltd.

Recruiting

Phase 2 Clinical Trial of CartiLife® in the United States

Articular Cartilage Defect | Articular Cartilage Degeneration

United States
Centre Hospitalier Universitaire Dijon

Completed

Treatment of Cirrhosis-related Hepatocellular Carcinoma With the Intrahepatic Arterial Injection of an Emulsion of Lipiodol and Idarubicin (Zavedos®): Phase I Study

Unresectable Non-metastatic Hepatocellular Carcinoma | Child A/B7 Cirrhosis

France
University of Luebeck

Unknown

Full Disclosure Observational Cardiac Rhythm Documentation Follow-up After Surgical Atrial Fibrillation Therapy

Atrial Fibrillation

Germany
University of Jena
Boston Scientific Corporation; Abbott Medical Devices; B. Braun Melsungen AG

Completed

Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everolimus-Eluting Coronary Stents (OCTOPUS)

Stents | Neointimal Proliferation

Germany
Indonesia University

Recruiting

Potential Use of Autologous and Allogeneic Mesenchymal Stem Cells in Patients With Multiple System Atrophy

Parkinsonism | Multiple System Atrophy | Multiple System Atrophy, Parkinson Variant

Indonesia
The University of Texas Health Science Center,...

Active, not recruiting

Subacromial Bursa Re-Implantation After Rotator Cuff Repair

Rotator Cuff Injuries

United States
Thuasne
International Clinical Trials Association

Recruiting

Auto-Adjustable MOBIDERM® Autofit NIGHT-time Compression Armsleeve in the Upper Limb LYMphedema in Maintenance Phase (LYMphoNIGHT)

Lymphedema of Upper Arm

France, Turkey
Karolinska University Hospital
DJO Incorporated; Region Stockholm

Completed

Compression Treatment Effects on Complications and Healing of Achilles Tendon Rupture

Rupture | Venous Thrombosis | Venous Thromboembolism | Surgical Wound Infection

Sweden
CVRx, Inc.

Completed

Rheos Feasibility Trial

Hypertension
Biosolution Co., Ltd.

Active, not recruiting

Phase 3 Clinical Trial of CartiLife® in Korea

Articular Cartilage Defect | Articular Cartilage Degeneration

Korea, Republic of
Abbott Medical Devices

Completed

QuickFlex Micro Left Ventricular Lead Post Approval Study

Heart Failure

United States
Krishnadevaraya College of Dental Sciences & Hospital

Completed

Evaluation of Self-filling Osmotic Tissue Expander in Augmenting Keratinized Tissue Around Dentulous Region

Soft Tissue Augmentation
Memorial Sloan Kettering Cancer Center

Active, not recruiting

Respiratory Motion-Corrected Cone-Beam CT and Intratreatment Gating Based on Electromagnetic Transponders to Reduce Target Position Uncertainty in Radiation Treatment of Lung Malignancies

Lung Cancer

United States
pfm medical ag
Aix Scientifics

Completed

Safety and Effectiveness of the Nit-Occlud® Lê VSD Spiral Coil System (pfm-01/2005)

Heart Septal Defects, Ventricular

Germany, Israel
Aesculap AG
Raylytic GmbH

Recruiting

In-vivo Wear Behaviour of AS Coated Versus Uncoated Columbus® Total Knee Prosthesis (COLRAS)

Knee Osteoarthritis | Osteonecrosis | Knee Arthritis | Instability, Joint | Rheumatoid Arthritis of Knee | Deformity Knee | Primary Osteoarthritis of Knee Nos | Secondary Osteoarthritis of Knee Nos

Australia, Germany
Tetec AG

Active, not recruiting

Phase III Study to Evaluate Safety and Effectiveness of NOVOCART 3D Plus vs. Microfracture in Knee Cartilage Defects (N3D)

Traumatic Articular Cartilage Defects in the Knee Joint

United Kingdom, Hungary, Czechia, Germany, Lithuania, Austria, France, Latvia, Poland, Switzerland
Global Stem Cell Center, Baghdad

Recruiting

Bone Marrow Cells With Core Decompression for AVN Treatment

Avascular Necrosis of the Femoral Head

Iraq
Medtronic Cardiovascular

Completed

Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement

Severe Aortic Stenosis

United States
ClarVista Medical

Completed

Evaluation of the Safety and Performance of the HARMONI® Toric Lens

Cataract | Corneal Astigmatism | Aphakia

New Zealand
Medical College of Wisconsin
SPIO

Recruiting

Orthosis to Improve Trunk Control in Infants Age 6-18 Months

Cerebral Palsy

United States
Imperial College London
Cambridge University Hospitals NHS Foundation Trust; University of Edinburgh; University of Manchester and other collaborators

Terminated

Decellularised Dermis Allograft for the Treatment of Chronic Venous Leg Ulceration (DAVE)

Venous Ulcer | Allograft

United Kingdom

Search clinical trials for: Core decompression/PREOB® implantation

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