Search clinical trials for: Survanta®

Total 13738 results

Alan Fujii
Dey LP

Terminated

Curosurf and Survanta Treatment(CAST)of RDS in Very Premature Infants (CAST)

Respiratory Distress Syndrome | Patent Ductus Arteriosus | Prematurity

United States
University of Michigan
Cornerstone Pharmaceuticals

Withdrawn

Comparison in Pulmonary Compliance Between Curosurf and Survanta in Preterm Infants With Respiratory Distress Syndrome

Respiratory Distress Syndrome

United States
NICHD Neonatal Research Network

Completed

Exosurf Neonatal and Survanta for Treatment of Respiratory Distress Syndrome (Surfactant 1)

Bronchopulmonary Dysplasia | Infant, Small for Gestational Age | Infant, Premature | Infant, Low Birth Weight | Infant, Newborn

United States
Sood, Beena G., MD, MS

Completed

Aerosolized Surfactant in Neonatal RDS (AS-02)

Respiratory Distress Syndrome, Newborn

United States
NICHD Neonatal Research Network
National Center for Research Resources (NCRR)

Terminated

Early Surfactant to Reduce Use of Mechanical Breathing in Low Birth Weight Infants (Surfactant 2)

Respiratory Insufficiency | Respiratory Distress Syndrome | Infant, Newborn

United States
Dr. Sami Ulus Children's Hospital

Completed

Comparison of Two Different Natural Surfactants in the Treatment of Pulmonary Hemorrhage

Pulmonary Hemorrhage

Turkey
Dr. Sami Ulus Children's Hospital

Completed

Perfusion Index Variability in Respiratory Distress Syndrome

Poor Peripheral Perfusion
Econometría Consultores
Inter-American Development Bank

Completed

Impact Evaluation of Training Civil Servants on Violence Against Women in Medellín, Colombia

Violence Against Women (VAW)

Colombia
Ramesh K Agarwal
All India Institute of Medical Sciences, New Delhi; Wellcome Trust; Lady Hardinge... and other collaborators

Unknown

Efficacy and Safety of Goat Lung Surfactant for the Treatment of Respiratory Distress Syndrome in Preterm Neonates

Respiratory Distress Syndrome
University of Sao Paulo
Ministry of Health, Brazil

Completed

A Multicenter, Randomized, Open Label Trial of a New Animal Extracted Surfactant to Treat RDS in Preterm Infants

Respiratory Distress Syndrome

Brazil
China Medical University, China
National Taiwan University Hospital; Chang Gung Memorial Hospital; Taipei Medical... and other collaborators

Unknown

Prevention of Chronic Lung Disease (CLD) in Preterm Infants

Respiratory Distress Syndrome | Chronic Lung Disease of Prematurity

China
Dong-A ST Co., Ltd.

Completed

A Study to Demonstrate the Efficacy and Safety of Motilitone®

Functional Dyspepsia

Korea, Republic of
Galderma R&D

Completed

Cetaphil Restoraderm Effect on Young Children With Atopic Dermatitis

Atopic Dermatitis

Philippines, China
Chong Kun Dang Pharmaceutical

Completed

CKD-391 DDI : Atorvastatin and Ezetimibe in Healthy Volunteers

Healthy

Korea, Republic of
Amir Azarpazhooh
Institut Straumann AG

Completed

Effect of Emdogain® on Soft Tissue Wound Healing

Periodontal Inflammation | Crown Lengthening

Canada
Novartis Pharmaceuticals

Completed

Inspiratory Flow Rates Achieved by the COPD Patients Through Breezhaler®, Ellipta® and Handihaler® Inhaler Devices

Pulmonary Disease, Chronic Obstructive (COPD)

Argentina
Guerbet

Completed

Efficacy Evaluation of Dotarem®-Enhanced MRI Compared to Gadovist®/Gadavist®-Enhanced MRI in the Diagnosis of Brain Tumors (REMIND)

Primary Brain Tumor

Colombia, Korea, Republic of, United States, Mexico
Sanofi Pasteur, a Sanofi Company

Completed

Safety and Immune Response of Different Pediatric Combination Vaccines.

Pertussis | Diphtheria | Polio

United States
Chung-Ang University Hosptial, Chung-Ang University...

Unknown

A Study to Evaluate the Efficacy Between Helicobacter Pylori Eradication Therapy and Motilitone in Functional Dyspepsia

Functional Dyspepsia

Korea, Republic of
University of Miami
BSN Medical Inc

Recruiting

VLU Dressing Study

Venous Leg Ulcer

United States
Sanofi Pasteur, a Sanofi Company

Completed

Rates of Pertussis Disease Among Persons Receiving Pentacel® or Other Pertussis Vaccines

Pertussis

United States
Coopervision, Inc.

Completed

Clinical Evaluation of Biofinity Multifocal Compared With Air Optix Aqua Multifocal and With PureVision Multifocal (INNOVATION)

Presbyopia
Tufts University

Completed

Comparison of Post Tooth Extraction Healing Using Different Xenograft Materials

Alveolar Bone Loss

United States
Assistance Publique Hopitaux De Marseille

Completed

Clinical Evaluation of the Treatment of Intellectual Metastases by Radiosurgery Gamma Knife by Means of a Support System by Mask. (Mask)

Lung Cancer | Brain Metastases

France
Global Kinetics Corporation

Withdrawn

Utilization of Target Ranges to Treat Persons With Parkinson's Disease by Objective Measurement Using the PKG (TARGET-PwP)

Parkinson Disease
University Hospital, Caen

Completed

Incidence of Dual Mobility Polyethylene Wear in Total Hip Prosthesis. Randomised Study Versus Fixed Insert by Radiostereometric Analysis. (DOUMOB)

Total Hip Replacement
Chiesi Farmaceutici S.p.A.

Completed

Pharmacokinetic Study of Bramitob® Administered for Inhalation by PARI eFlow® vs PARI LC® PLUS Nebulizer

Cystic Fibrosis

Czechia, Moldova, Republic of, Slovakia
Hoffmann-La Roche

Completed

A Study to Assess All-Cause Mortality and Cardiovascular Morbidity in Participants With Chronic Kidney Disease (CKD) on Dialysis and Those Not on Renal Replacement Therapy Receiving Methoxy Polyethylene Glycol-Epoetin Beta (Mircera) or Reference Erythropoietin Stimulating Agents (ESAs)

Chronic Renal Anemia

Belgium, Brazil, United Kingdom, Serbia, Spain, Germany, Korea, Republic of, Turkey, Lithuania, Italy, Czechia, Argentina, Australia, Croatia, France, Greece, Israel, Malaysia, Mexico, Panama, Philippines, Poland, Russian Federation, ... and more
Global Kinetics Corporation

Terminated

Utilization of Target Ranges to Treat Parkinson's Disease With the PKG (TARGET-PD)

Parkinson Disease

United States
nthalmic Pty Ltd
Brighten Optix Corporation

Recruiting

S.T.O.P.® Technology Contact Lenses Versus Dual-focus Contact Lenses for Slowing Down Myopia Progression in Children

Myopia

India, Spain, China
Lument AB

Terminated

A Randomized, Controlled Trial to Evaluate CT Image Quality Lumentin® 44

Subjects Referred to CT-examination of the Abdomen

Sweden
W.L.Gore & Associates

Completed

GORE® TAG® Thoracic Endoprosthesis French Mandatory Registry

Aortic Diseases | Aortic Aneurysm, Thoracic | Penetrating Ulcer | Descending Thoracic Aortic Dissection | Aorta Thoracic; Traumatic Rupture

France
Revance Therapeutics, Inc.

Active, not recruiting

Teosyal RHA® Histology and Intradermal Implantation Evaluation Study

Histology

Canada
Tufts University

Completed

Effect of Mucograft® Seal on Post-extraction Ridge Preservation Using Bone Allograft (Mucograft)

Tooth Extraction Status Nos
CereVasc Inc
AlvaMed, Inc.; Simplified Clinical Data Systems, LLC; Bioscience Consulting,...

Terminated

Pilot Study to Evaluate the CereVasc® eShunt® System in the Treatment of Communicating Hydrocephalus

Hydrocephalus | Hydrocephalus, Communicating

United States
University of Baghdad

Completed

Evaluating Implant Stability Using Three Devices Osstell®, Periotest® and AnyCheck®

Edentulous Alveolar Ridge

Iraq
Novo Nordisk A/S

Completed

A Trial to Investigate the Bioequivalence of Norditropin® (Somatropin) Versus Genotropin® (Somatropin) in Healthy Adult Subjects

Healthy | Growth Disorder

United States
Almirall, S.A.
Forest Laboratories

Completed

Preference, Satisfaction and Ease of Use of Genuair® (Pressair™) and Breezhaler® (Neohaler™) Inhalers in Patients With COPD

Chronic Obstructive Pulmonary Disease (COPD)

Germany, Spain, United Kingdom
Guangzhou Institute of Respiratory Disease

Completed

Carbon Dioxide Rebreathing During Exercise Assisted by Non-invasive Ventilation

Pulmonary Disease, Chronic Obstructive

China
Université de Montréal

Completed

Peri-Implant Healing Around Two Different Machined-Collar Designs After 25 Years of Function

Jaw, Edentulous

Canada
CVRx, Inc.

Completed

Rheos System for the Treatment of HFpEF Heart Failure (HOPE4HF)

Heart Failure

United States
W.L.Gore & Associates

Suspended

GORE® VIABIL® Biliary Endoprosthesis in the Treatment of Benign Biliary Strictures Secondary to Chronic Pancreatitis (VIABILITY)

Pancreatitis, Chronic | Stricture; Bile Duct

United States
Guerbet

Completed

Xenetix® 350: Comparative Assessment of Image Quality for Coronary CT Angiography (X-ACT)

Coronary Artery Disease

Spain, France, Germany, Italy, Switzerland
Novartis Pharmaceuticals

Completed

Six Months Efficacy and Safety of Aliskiren Therapy on Top of Standard Therapy, on Morbidity and Mortality in Patients With Acute Decompensated Heart Failure (ASTRONAUT)

Acute Decompensated Heart Failure | Congestive Heart Failure

Colombia, Czech Republic, India, Italy, Belgium, Turkey, Argentina, France, Germany, Israel, Spain, Canada, Taiwan, United States, Singapore, Russian Federation, Philippines, Slovakia, Sweden, Hungary, Finland, Poland, Romania, Brazil
Pharmacosmos A/S

Completed

Incidence of Hypophosphatemia After Treatment With Iron Isomaltoside/Ferric Derisomaltose vs Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia

Iron Deficiency Anemia | Iron Deficiency Anaemia

United States
Ascensia Diabetes Care

Completed

Comparison Evaluation of Blood Glucose Meter Systems

Diabetes

United States
Seung-Jung Park
CardioVascular Research Foundation, Korea

Withdrawn

Star-Close Versus Angio-Seal for Femoral Artery Hemostasis (CLOSE)

Percutaneous Intervention Via Femoral Artery

Korea, Republic of
Groupe Mulliez-Flory
EVAMED

Recruiting

Evaluation of Safe Use of SECURIDRAP® SELFIA® (SECURIDRAP)

Cognitive Impairment | Behavior Disorders | Disorientation

France
University Hospital, Strasbourg, France

Recruiting

Evaluation of a New Predictive Test of Preterm Birth in Case of Threatened Preterm Labor (PREMAQUICK)

Preterm Delivery | Threatened Preterm Labor

France
Vastra Gotaland Region

Completed

A Comparison Between Biological (Veritas®) vs Non Biological Mesh (TIGR®) in Immediate Breast Reconstruction

Breast Cancer

Sweden

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