Search clinical trials for: ALLOB® implantation

Total 14979 results

Bone Therapeutics S.A

Completed

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

Long Bone Delayed-Union Fracture
Mayo Clinic

Active, not recruiting

REcycled CartiLage Auto/Allo IMplantation

Cartilage Defect

United States
Bone Therapeutics S.A

Terminated

Study on Allogeneic Osteoblastic Cells Implantation in Rescue Interbody Fusion

Failed Lumbar Fusion

Belgium
Instituto de Molestias Cardiovasculares
Medtronic

Unknown

Stem Cells and Resynchronization Cardiac (RCT and SCT)

Heart Failure

Brazil
Perouse Medical
Eclevar Medtech

Completed

Safety and Performance of POLYTHESE® Vascular Prosthesis

Peripheral Arterial Disease | Marfan Syndrome | Ehlers-Danlos Syndrome | Aneurysm Arterial | Arterial Dissections

France
Wenzhou Medical University

Not yet recruiting

Influence of Capsular Tension Ring on IOL-capsular Complex After Cataract Surgery in Patients With High Myopia: a Clinical Observation Based on SS-OCT

Capsular Tension Ring | High Myopia

China
Aesculap AG

Completed

Comparative Study of AESCULAP Optilene® Mesh Elastic Versus Ethicon Ultrapro® Mesh in Incisional Hernia Repair (Optilene)

Incisional Hernia Repair

Germany
NeuroPace

Completed

RNS® System Feasibility Study

Epilepsy

United States
NeuroPace

Completed

RNS® System Pivotal Study

Epilepsy

United States
Bone Therapeutics S.A

Completed

Phase 2a Study on Allogeneic Osteoblastic Cells Implantation in Lumbar Spinal Fusion

Degenerative Disc Disease

Belgium
Swiss Vision Network

Active, not recruiting

Longitudinal Study on Glaucoma Surgery Using XEN® Gel Stent

Glaucoma | Glaucoma, Open-Angle | Glaucoma, Angle-Closure | Glaucoma, Primary Open Angle
pfm medical ag
Aix Scientifics; Crolll Gmbh; Bayes GmbH; GfE Medizintechnik GmbH; pfm medical titanium...

Completed

Anterior Pelvic Prolapse Reconstruction With TiLOOP® Total 6

Cystocele | Uterine Prolapse

Germany
Cantonal Hospital of St. Gallen

Terminated

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

Abdominal Aortic Aneurysm

Switzerland
Affiliated Hospital of Hebei University

Unknown

Cobalt Alloy Pedicle Screw Implantation for Severe Kyphosis Deformity in Spinal Tuberculosis

Spinal Tuberculosis
Erasme University Hospital
University of Liege; Bone Therapeutics S.A

Completed

Autologous Osteoblastic Cells Implantation to Early Stage Osteonecrosis of the Femoral Head (PREOB-ON2)

Avascular Necrosis of Femur Head

Belgium
Bone Therapeutics S.A

Terminated

Study on Autologous Osteoblastic Cells Implantation to Early Stage Osteonecrosis of the Femoral Head

Osteonecrosis of the Femoral Head
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
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
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
Sahlgrenska University Hospital, Sweden

Completed

Microembolic Signals and Serum Markers of Neuronal Damage During Transcatheter Aortic Valve Implantation.

Aortic Stenosis

Sweden
Biosolution Co., Ltd.

Recruiting

Phase 2 Clinical Trial of CartiLife® in the United States

Articular Cartilage Defect | Articular Cartilage Degeneration

United States
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
Biosolution Co., Ltd.

Active, not recruiting

Phase 3 Clinical Trial of CartiLife® in Korea

Articular Cartilage Defect | Articular Cartilage Degeneration

Korea, Republic of
Bone Therapeutics S.A

Terminated

Study on Autologous Osteoblastic Cells Implantation in Hypotrophic Non-Union Fractures

Long Bone Non-Union

Belgium, France, Netherlands
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
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
Bone Therapeutics S.A
ICON plc

Recruiting

Study to Assess the Efficacy and Safety of Allogeneic Osteoblastic Cells (ALLOB®) Single Implantation in Tibial Fracture (ALLOB-TF2)

Tibial Fracture

Belgium, Czechia, France, Germany, Hungary, Poland, Spain
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
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
University Hospital, Clermont-Ferrand
LivaNova; Biotronik France

Unknown

Assessment of the Prognosis of Persistent Left Bundle Branch Block (LBBB)After Transcatheter Aortic Valve Implantation (TAVI ) by an Electrophysiological and Remote Monitoring Risk-adapted Algorithm (LBBB-TAVI)

Post-TAVI

France
Anterogen Co., Ltd.

Recruiting

A Study to Evaluate the Safety of ALLO-ASC-CD for Treatment of Crohn's Disease

Crohn's Disease

Korea, Republic of
Bausch & Lomb Incorporated

Completed

Evaluation of Clinical Outcomes Following Implantation of a Sub-2mm Hydrophilic MICS Intraocular Lens

Cataract

France
Vissum, Instituto Oftalmológico de Alicante
Instituto de Salud Carlos III; Universidad Miguel Hernandez de Elche

Completed

Autologous Adipose-Derived Adult Stem Cell Implantation for Corneal Diseases (ADASCs-CT-CD) (ADASCs-CT-CD)

Keratoconus | Treatment | Therapy | Corneal Dystrophy | Ophthalmological Disorder

Spain
Assistance Publique - Hôpitaux de Paris
Ministry of Health, France

Recruiting

Cardioverter DefIbriIlator PlacEMent for priMary Prevention of Sudden cArdiac Death in Patients Older Than 75 Years (DILEMMA)

Heart Failure | Implantable Cardioverter Defibrillator | Primary Prevention of Sudden Cardiac Death

France
Sunnybrook Health Sciences Centre

Recruiting

Anterior Chamber Versus Scleral Fixated Intraocular Lens: Long-term Vision and Safety Outcomes

Corneal Endothelial Cell Loss | Secondary Intraocular Lens

Canada
Central Hospital, Nancy, France

Active, not recruiting

Implantation of Continent Catheterizable Channel : Native Bladder or Enterocystoplasty ? (ICODE)

Neurogenic Bladder | Continent Cutaneous Urinary Diversion | Mitrofanoff

France
Yong-Mei Cha

Recruiting

His Bundle Pacing in Bradycardia and Heart Failure

Heart Failure | Bradycardia

United States
Meshalkin Research Institute of Pathology of Circulation

Completed

Comparison of Rigid Annuloplasty Ring With a Band in the Correction of Secondary Tricuspid Insufficiency (BvsRR)

Tricuspid Regurgitation

Russian Federation
Helios Health Institute GmbH
Heart Center Leipzig - University Hospital

Terminated

Re-evaluation of Optimal Re-synchronisation Therapy in Patients With Chronic Heart Failure (RESET-CRT)

Chronic Heart Failure

Germany
Beaver-Visitec International, Inc.

Completed

Comparison of Clinical Outcomes POD L GF vs POD F GF (PHY1707)

Cataract | Presbyopia | Lens Opacity

Hungary
yin ying zhao

Completed

Inflammatory Cytokines in Congenital Cataract After Lensectomy and Anterior Vitrectomy

Congenital Cataract

China
Beaver-Visitec International, Inc.

Completed

Comparison of Visual Outcomes After Implantation of the POD AY GF F (PhysIOL) and the POD AY 26P F (PhysIOL)

Cataract | Lens Opacity

Hungary

Search clinical trials for: ALLOB® implantation

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