Search clinical trials for: Ambu® AuraGain™

Total 13853 results

Biosense Webster, Inc.

Terminated

Efficacy, Safety and Efficiency Study of CARTO® 3 System Guided THERMOCOOL® Catheter Ablation Versus Fluoroscopy Guided Ablation With the Pulmonary Vein Ablation Catheter® (PVAC®) (CLARITY-AF)

Atrial Fibrillation

Netherlands, Belgium, Canada, Denmark, Germany, United Kingdom
Medical University of Graz

Terminated

Proof of Concept: Socket Seal (SocketSeal)

Tissue Preservation

Austria
Alcon Research

Completed

Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems

Refractive Error | Astigmatism | Myopia

United States
PathMaker Neurosystems Inc.
National Institute of Neurological Disorders and Stroke (NINDS); Spaulding...

Recruiting

Study Evaluating MyoRegulator® Treatment in Post-Stroke Upper Limb Spasticity (RECOVER)

Stroke | Muscle Spasticity

United States
Jules Bordet Institute

Not yet recruiting

Efficacy of the Mepitel® Film on the Prevention of Radiodermatitis in the Inguinal Fold.

Radiation Toxicity | Radiodermatitis | Radiotherapy Side Effect
Labo'Life

Recruiting

Study to Evaluate the Efficacy of 2LEBV® and 2LXFS® on Asthenia in Patients With an Epstein-Barr Virus Infection (EBVAST)

EBV Infection

Belgium
GCS Co., Ltd
Eurofins Dermscan Pharmascan

Active, not recruiting

Clinical Study for the Evaluation of the Safety and Effectiveness of Use of a Poly-L Lactic Acid Injectable Filler for the Aesthetic Treatment of Nasolabial Folds (PLLA)

Wrinkle

France
W.L.Gore & Associates

Completed

GORE® VIABAHN® Endoprosthesis Post-Marketing Surveillance Study (JPS 16-03)

Peripheral Arterial Disease

Japan
Northern California Research Trials, Inc.
Pacira Pharmaceuticals, Inc; NorthBay Healthcare

Active, not recruiting

Cryoanalgesia for the Treatment of Pain in Subjects With Morton's Neuroma

Pain Management | Morton's Neuroma

United States
W.L.Gore & Associates

Completed

Evaluation of the GORE® VIABAHN® Endoprosthesis for the Treatment of Popliteal Artery Aneurysm (PAA)

Popliteal Artery Aneurysm

France
Medtronic Cardiac Rhythm and Heart Failure

Completed

Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Trials (HW-PAS-03)

Heart Failure

United States
University of Zurich

Completed

Exercise and Oscillatory Positive Expiratory Pressure Therapy in Cystic Fibrosis

Cystic Fibrosis

Switzerland
Biosense Webster, Inc.

Completed

Catheter Evaluation for Endocardial Ablation in Patients With Ventricular Tachycardia (VT-CoA)

Ventricular Tachycardia

United States
OcuNexus Therapeutics, Inc.

Terminated

The ASCEND Study: A Study to Investigate the Safety and Clinical Effect of Nexagon to Treat Slow Healing Diabetic Foot Ulcers

Diabetic Foot Ulcer

New Zealand
University of Heidelberg Medical Center
Heidelberg Engineering GmbH

Recruiting

Evaluation of Optical Coherence Tomography in Dentistry

Dental Caries | Tooth Demineralization

Germany
OcuNexus Therapeutics, Inc.

Completed

A Study to Investigate the Efficacy, Safety and Tolerability of Nexagon® as a Topical Treatment for Subjects With Venous Leg Ulcers (NOVEL2)

Venous Leg Ulcers

United States, New Zealand, South Africa, Australia
Becton, Dickinson and Company

Completed

Evaluating the User Performance and Experience of Nucleus Pen vs. Commercially Available Pen Needle

Diabetes

United States
Abiomed Inc.

Recruiting

Impella®-Supported PCI in High-Risk Patients With Complex Coronary Artery Disease and Reduced Left Ventricular Function (PROTECT IV)

Coronary Artery Disease | Left Ventricular Dysfunction

United States, Switzerland, Germany, Canada, Italy, Netherlands, United Kingdom
Berlin Heart, Inc

Approved for marketing

Assess Safety and Probable Benefit of the EXCOR® Pediatric Ventricular Assist Device Under a Continued Access Protocol (CAP)

Heart Failure | Cardiomyopathies
Pharmacosmos A/S

Completed

An Extension Trial to Assess the Safety of Re-dosing of Iron Isomaltoside/Ferric Derisomaltose (Monofer®/Monoferric®) (FERWON-EXT)

Iron Deficiency Anemia | Iron Deficiency Anaemia

United States
Daniel S. Durrie, MD
Alcon Research

Completed

Visual Outcomes and Contrast Sensitivity After Myopic LASIK

Myopia

United States
Alcon Research

Completed

Comparison of Two Daily Disposable Lenses

Myopia | Refractive Ametropia

United States
Mylan Inc.
Cystic Fibrosis Foundation

Completed

Observational Study in Cystic Fibrosis Patients Using TOBI® PODHALER® or Other FDA Approved Inhaled Antipseudomonal Antibacterial Drugs

Pseudomonas Aeruginosa in Cystic Fibrosis

United States
Dentsply Sirona Implants

Completed

Study Comparing Appearance and Function of Three Different Dental Implant Designs When Placed in Front Region of Upper Jaw

Jaw, Edentulous, Partially

United States, Canada
CIBA VISION
University of Waterloo

Completed

Lens Wear Schedules and End-of-Day Comfort (INVERMERE)

Myopia

Canada
M.D. Anderson Cancer Center

Recruiting

A Pilot Study for Pupillary Assessment to Predict CAR-T Related Neurotoxicity

Neurotoxicity

United States
Perrigo CSCI

Recruiting

Comparative Study for the Evaluation of Two Medical Devices on the Treatment of Head Lice Infestation

Head Lice Infestation

Mauritius
Uludag University

Not yet recruiting

Which Technique is Effective in Reducing the Pain of Peripheral Intravenous Catheterization in Pediatric Patients, Infra-Red Light or Buzzy®?

Pain Management
Roquette Frères
BioFortis

Completed

The Effects of Daily Supplementation of Nutriose® on the Fecal Microbiota in Volunteers. (NUTRIBIOTE)

Healthy Male Volunteers

France
Medinol Ltd.

Terminated

ChampioNIR® SFA Stent EFS Study

Peripheral Arterial Disease

Israel
Liaquat University of Medical & Health Sciences

Completed

Assessing Success of MTA and Pre-mixed Bioceramic in Mature Teeth With Irreversible Pulpitis With Full Pulpotomy. (GCP)

Pulpitis - Irreversible

Pakistan
Genzyme, a Sanofi Company

Completed

Growth and Development Study of Alglucosidase Alfa

Glycogen Storage Disease Type II (GSD-II) | Acid Maltase Deficiency Disease | Pompe Disease

United States
W.L.Gore & Associates

Completed

Removable GORE VIABIL® Biliary Endoprosthesis for Treatment of Benign Biliary Strictures

Biliary Strictures

Germany
Peking Union Medical College Hospital
Beijing Chao Yang Hospital; Beijing Obstetrics and Gynecology Hospital; San MediTech(Huzhou)Co... and other collaborators

Unknown

Nutrition Product Combine With Continuous Glucose Monitoring in Gestational Diabetes Mellitus Patients

SANZ®KINGWILL Combined With CGM Equipment in GDM Patients | GLUCERNA SR® Combined With CGM Equipment in GDM Patients

China
Johns Hopkins University
Ohio State University; Henry Ford Health System; Rhode Island Hospital; Virginia... and other collaborators

Completed

A Randomized Cross-over Study for Normal Pressure Hydrocephalus (ARCS NPH)

Normal Pressure Hydrocephalus

United States
W.L.Gore & Associates

Completed

Long-term Safety Study of the GORE® HELEX® Septal Occluder

Septal Defect, Atrial

United States
Ulthera, Inc

Completed

Ultherapy® for the Treatment of Acne Scars

Acne Scars | Atrophic Acne Scars

United States
Ulthera, Inc

Terminated

Peri-orbital and Peri-oral Wrinkle Reduction Trial

Peri-oral Wrinkles | Peri-orbital Wrinkles

United States
EndoChoice Inc.

Completed

Exploratory Study of Upper and Lower Endoscopic Fuse System

Gastrointestinal Diseases
University of Cologne

Completed

Performance of Flexible Self-adherent Absorbent Dressing Coated With a Soft Silicone Layer After Hip -,Knee- Arthroplasty,Primary Spine Surgery in Comparison to a Standard Wound Dressing (wounddressing)

Spine Surgery | Hip-arthroplasty | Knee-arthroplasty

Germany
W.L.Gore & Associates

Completed

Evaluation of the 25 Centimeter (cm) GORE® VIABAHN® Endoprosthesis

Peripheral Vascular Diseases
University of Zurich

Completed

The Effects of Provent® on Obstructive Sleep Apnea During Continuous Positive Airway Pressure Therapy Withdrawal

Obstructive Sleep Apnea

Switzerland, United Kingdom
AstraZeneca

Terminated

A Multiple Ascending Dose Study With AZD9164 Given for 13 Days in Healthy Male and Female Subjects and in Patients With Chronic Obstructive Pulmonary Disease

Healthy | COPD

Sweden
Ospedale San Donato
Ospedale Le Scotte; Ospedale della Misericordia - Grosseto

Completed

Comparison Between Iso-Osmolar and Ipo-Osmolar Contrast Agents in Patients With Acute Myocardial Infarction (AMI) Undergoing Primary Percutaneous Coronary Intervention (PCI) (CONTRAST-AMI)

Acute Myocardial Infarction | Contrast Induced Nephropathy

Italy
Alcon Research

Completed

Visual Function After Implantation of Bilateral AcrySoft ReSTOR Aspheric IOL

Cataract

United States
Aesculap AG

Completed

Trial to Evaluate the Hemostatic Effect of Lyostypt® Versus Surgicel® in Arterial Bypass Anastomosis (COBBANA)

Peripheral Vascular Diseases | Hemostasis

Germany
FinnMedi Oy
Tampere University; The Laboratory and Pharmacy Public Utility of the Pirkanmaa...

Completed

The Effects of Preservative-free Prostaglandin Eye Drops in Sign and Symptoms on the Eyes of Patients With Glaucoma

Ocular Hypertension | Open-Angle Glaucoma

Finland
GlaxoSmithKline

Completed

Immunogenicity, Safety and Reactogenicity Study of GlaxoSmithKline (GSK) Biologicals' Hib-MenCY-TT (MenHibrix®) Vaccine Compared to Merck & Co, Inc. PedvaxHIB Vaccine in Healthy Infants and Toddlers 12 to 15 Months of Age

Neisseria Meningitidis | Haemophilus Influenzae Type b

United States
HLT Inc.

Withdrawn

HLT® Meridian® TAVR Valve System Early Feasibility Study for Aortic Regurgitation (RIVAL - AR EFS)

Aortic Regurgitation

United States
Weill Medical College of Cornell University
King Systems Corporation; KARL STORZ Endoscopy-America, Inc.

Completed

Comparison Study in Adult Surgical Patients of 5 Airway Devices

Intubation | Laryngoscopy

3

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