Search clinical trials for: CellMist™ System

Total 80777 results

Vectorious Medical Technologies Ltd.

Recruiting

V-Lap System For Wirelessly Measuring And Monitoring Left Atrial Pressure (LAP) In Patients With Advance CHF

Heart Failure

Georgia
Vectorious Medical Technologies Ltd.

Recruiting

V-Lap System For Wirelessly Measuring And Monitoring Left Atrial Pressure (LAP) In Patients With Advance Chronic Heart Failure

Heart Failure

Israel
Xiros Ltd

Recruiting

PMCF Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair

Achilles Tendon Rupture

United Kingdom
Medtronic Cardiac Rhythm and Heart Failure

Recruiting

DIAMOND AF Post-Approval Study (DAF PAS)

Paroxysmal Atrial Fibrillation

United States, France, Italy, Greece
CVRx, Inc.

Recruiting

BAROSTIM THERAPY™ In Resistant Hypertension

Hypertension

Germany, Netherlands
CVRx, Inc.

Recruiting

BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction (HFpEF)

Heart Failure

Germany
Medtronic - MITG

Completed

A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapling System.

Thoracic Diseases | Abdominal Injury

United States, Spain, Canada, Italy, United Kingdom
Intuitive Surgical

Active, not recruiting

Clinical Utility for Ion Endoluminal System

Lung Diseases | Lung Cancer | Pulmonary Nodule

United States
Anteris Technologies Ltd.

Active, not recruiting

DurAVR™ THV System: First-In-Human Study

Aortic Valve Calcification | Severe Aortic Valve Stenosis | Symptomatic Aortic Stenosis

Georgia
Candela Corporation

Active, not recruiting

Functional Usability and Feasibility Testing of the Profound Matrix™ System

Acne Scars - Mixed Atrophic and Hypertrophic | Wrinkle

United States, Israel
Poitiers University Hospital

Completed

Study Comparing Conventional, Burst and High Frequency (HF) Spinal Cord Stimulation (SCS) in Refractory Failed Back Surgery Syndrome (FBSS) Patients After a 32-contact Surgical Lead Implantation (MULTIWAVE)

Failed Back Surgery Syndrome

France
Sonendo, Inc.

Completed

Sonendo GentleWave™ System for Treatment in Molar Teeth Requiring Root Canal Therapy (SUPREME)

Root Canal Therapy

United States
DePuy International

Terminated

A Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-ceramic Bearing in Primary Total Hip Replacement

Osteoarthritis | Rheumatoid Arthritis | Avascular Necrosis | Post-traumatic Arthritis | Congenital Hip Dysplasia | Slipped Capital Femoral Epiphysis | Collagen Disorders | Traumatic Femoral Fractures | Nonunion of Femoral Fractures

Czech Republic
DePuy International

Terminated

A Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-Metal or a Metal-on-Metal Bearing

Osteoarthritis | Avascular Necrosis | Post-traumatic Arthritis | Congenital Hip Dysplasia | Slipped Capital Femoral Epiphysis | Collagen Disorders

Germany
MedtronicNeuro

Completed

Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression

Depression

United States
Rennes University Hospital

Completed

Management of Obstructive Sleep Apnea (OSA) in Children and Maxillary and Mandibular Development (SAOS)

Obstructive Sleep Apnea Syndrome

France
Taichung Veterans General Hospital

Completed

HFCWO in Prolonged Mechanical Ventilation Patients

Chronic Ventilator Dependency

Taiwan
Symetis SA

Completed

PRospective Observation of Aortic reGuRgitation aftEr TAVI and progreSS Over Time: PROGRESS PVL Registry (PROGRESS)

Aortic Stenosis

Germany, Canada, Italy, United Kingdom
MedtronicNeuro

Recruiting

Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study (EPAS) (EPAS)

Epilepsy

United States, Belgium, Czechia, Portugal
Teva Neuroscience, Inc.
Teva Branded Pharmaceutical Products R&D, Inc.; TransPharma Medical

Completed

A Multi-Dose Study to Assess Tolerability, Safety and Pharmacology of hGH-ViaDerm™ System in Adults With GH-Deficiency

Growth Hormone Deficiency
Meccellis Biotech

Completed

Safety and Performance Evaluation of a Biological Matrix Used for Rectal Prolapse Repair by Ventral Rectopexy

Rectal Prolapse

France
Field Medical

Recruiting

Ventricular Catheter Ablation Study (VCAS) (VCAS)

Ventricular Tachycardia | Ventricular Arrythmia | Ventricular Tachyarrhythmia | PVC - Premature Ventricular Complex | PVC - Premature Ventricular Contraction

Czechia
Orthofix Inc.

Terminated

Advent™ Cervical Disc Versus ACDF for Treatment of One Level Degenerative Disc Disease (IDE Study)

Cervical Degenerative Disc Disease

United States
Boston Scientific Corporation

Not yet recruiting

ADVENT Post-Approval Study (ADVENT PAS)

Paroxysmal Atrial Fibrillation
Symetis SA

Completed

ACURATE™ Transapical Aortic Bioprosthesis for Implantation in Patients With Severe Aortic Stenosis (2010-01) (TA-PILOT)

Aortic Symptomatic Stenosis

Germany
Cordis Corporation
NAMSA; Qserve

Completed

Evaluation of Safety and Efficacy of the S.M.A.R.T. RADIANZ™ Vascular Stent System in the Treatment of Iliac and Femoropopliteal Lesions Via Transradial Access (RADIANCY)

Peripheral Arterial Disease

France, Switzerland, Italy, Austria, Belgium, Spain
Smith & Nephew, Inc.

Active, not recruiting

Safety and Performance of MICRORAPTOR™ Suture Anchors in Shoulder and Hip

Acetabular Labrum Tear | SLAP Lesion | Bankart Lesions | Rotator Cuff Tears | Labral Tear, Glenoid | Anterior Shoulder Instability

United States
Nuvaira, Inc.

Completed

Targeted Lung Denervation for Patients With Moderate to Severe COPD (AIRFLOW)

Chronic Obstructive Pulmonary Disease (COPD)

France, Belgium, Netherlands, Austria, Germany, United Kingdom
Boston Scientific Corporation

Completed

China Greenlight Registry Study (Post-market)

Benign Prostatic Hyperplasia (BPH)

China
Abbott Medical Devices

Completed

IPG Replacement Study (PREFERENCE-H) (PREFERENCE-H)

Parkinson Disease

Italy, Germany, United States
Symetis SA

Completed

ACURATE TF™ Transfemoral Aortic Bioprosthesis for Implantation in Patients With Severe Aortic Stenosis:CE-approval Cohort

Symptomatic Aortic Stenosis

Germany, Japan, Brazil
Symetis SA

Completed

Feasibility Trial on ACURATE™ Transapical Implantation in Patients With Severe Symptomatic Aortic Stenosis (2009-01) (TA-FIM)

Aortic Stenosis Symptomatic

Germany
Medtronic Cardiac Surgery

Recruiting

CLIP-IT Post-Market Study

Left Atrial Appendage Exclusion

United States
Lifetech Scientific (Shenzhen) Co., Ltd.

Not yet recruiting

Cera™ Vascular Plug System Post-Market Clinical Follow-Up

Aneurysm | Portal Hypertension | Arteriovenous Fistula | Endoleak | Pulmonary Arteriovenous Malformation | Splenic Laceration
Boston Scientific Corporation

Completed

SpyGlass™ Discover Percutaneous

Pancreatic Diseases | Bile Duct Diseases | Bile Duct Obstruction

United States, Belgium, Italy, Canada, Germany, Hong Kong, India
Boston Scientific Corporation
Quintiles, Inc.

Withdrawn

REPRISE China - Clinical Evaluation in China

Stenoses, Aortic Valve

China
SoundBite Medical Solutions, Inc.
Montreal Heart Institute; ethica Clinical Research Inc.

Withdrawn

Prospective Study of the SoundBite™ Crossing System in Complex Peripheral CTOs (PROSPECTORII)

Peripheral Arterial Occlusive Disease | Chronic Total Occlusion of Artery of the Extremities

Austria, Germany
Amir Lerman

Completed

Feasibility and Efficacy of Coronary Sinus Narrowing in Patients With Coronary Microvascular Dysfunction (Reducer)

Coronary Microvascular Dysfunction

United States
Neurent Medical

Completed

Safety and Efficacy Study of the Neurent Medical NEUROMARK™ System in Subjects With Chronic Rhinitis (MERIDIEN)

Chronic Rhinitis

United States
Ulthera, Inc

Completed

Histological Analysis Following Ulthera System Treatment for Hyperhidrosis

Hyperhidrosis

United States
Ulthera, Inc

Completed

Feasibility Study: Higher Density Ulthera® System Treatment With Vectoring for Treatment of the Face and Neck

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Lifting and Tightening of the Elbows

Skin Laxity

United States
Ulthera, Inc

Completed

Feasibility Study: Ulthera Treatment of the Buttocks and Thighs

Skin Laxity

United States
Biomet Orthopedics, LLC

Completed

A Clinical Investigation of the C2a-Taper™ Acetabular System

Osteoarthritis | Avascular Necrosis | Congenital Hip Dysplasia | Traumatic Arthritis

United States
Renal Dynamics GmbH
Biosensors Europe SA; Physio-Logic Ltd. Israel; AmeRuss Clinical Trials LLC, USA

Unknown

A Study to Evaluate Safety and Efficacy of the Redy™ Renal Denervation System in the Treatment of Patients With Uncontrolled Hypertension

Hypertension Resistant to Conventional Therapy

Israel, Belgium, Germany, Hungary, Ireland, Poland, Russian Federation, Serbia
Meshalkin Research Institute of Pathology of Circulation

Completed

The SIBERIA Trial (Acculink™ Versus CGuard™) (CAS)

Patients With Aterosclerotic Carotid Stenosis | Symptomatic Patients (Stenosis > 50%) | Asymptomatic Patients (Stenosis ≥80%)

Russian Federation
Medtronic Endovascular

Completed

DURABILITY™ Iliac Study

Peripheral Arterial Disease | Claudication

United States
Western Galilee Hospital-Nahariya

Not yet recruiting

Effect of Intermittent Pneumatic Compression Device of Lower Limbs in Oligohydramnios

Oligohydramnios | Amniotic Fluid; Disorder
Zimmer Biomet

Active, not recruiting

A Clinical Investigation of the Vanguard™ Complete Knee System

Osteoarthritis | Rheumatoid Arthritis | Traumatic Arthritis | Lower Limb Deformity | Complications, Arthroplasty

United States
University Hospital, Saarland

Withdrawn

Renal Denervation in Patients With Chronic Heart Failure

Chronic Heart Failure | Cardio-Renal Syndrome

Austria, Germany, Switzerland, Sweden

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