Search clinical trials for: Hyzaar®

Total 13827 results

Alexion Pharmaceuticals
Portola Pharmaceuticals

Completed

Phase 1/2a Dose Escalation Study in Participants With CLL, SLL, or NHL

Follicular Lymphoma (FL/Indolent NHL) | Aggressive NHL (a NHL) | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | T-cell Lymphoma (PTCL and CTCL) | B-cell Non Hodgkin Lymphoma (NHL)

United States
Pharmacosmos A/S

Completed

Iron Isomaltoside/Ferric Derisomaltose vs Iron Sucrose for the Treatment of Iron Deficiency Anemia (IDA)

Iron Deficiency Anemia | Iron Deficiency Anaemia

United States
Institut National de la Santé Et de la Recherche...

Not yet recruiting

Prospective Study to Assess Medical Performance of Optical Mapping and Long Read Sequencing in Detecting Numerical and Structural Chromosome Abnormalities. CHROmosome MAPping and Sequencing (CHROMAPS)

Infertility | Intellectual Disability | Malformation
Can Tho Stroke International Services Hospital
Acandis GmbH

Completed

Credo Stent in the Symptomatic Intracranial Stenosis (CRESIS)

Ischemic Stroke | Stent Stenosis | Intracranial Atherosclerosis

Vietnam
Pfizer
Pfizer

Completed

Retrospective Real World Oxbryta® Data Collection and Analysis Study (RETRO)

Sickle Cell Disease

United States
W.L.Gore & Associates

Active, not recruiting

Evaluation of the GORE® TAG® Thoracic Branch Endoprosthesis (TBE Device) in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta (Zone 0/1) (SSB 11-02)

Aortic Aneurysm, Thoracic | Aorta, Lesion

United States, Japan
Canadian Memorial Chiropractic College

Completed

Effects of ART® on Lower Limb Myofascial Pain and Function

Lower Limb Injury | Muscle Injury

Canada
PD Dr. Jan Kottner

Completed

Effectiveness of Two Silicone Dressings for Sacral and Heel Pressure Ulcer Prevention

Pressure Ulcer

Germany
Bolton Medical

Completed

Global Post-market Registry for the Treovance Stent-graft. (RATIONALE)

Abdominal Aortic Aneurysm

Spain, Greece, Norway, Germany, Ireland, Sweden, Italy, Hong Kong, Thailand, Netherlands, Vietnam, Chile, United Kingdom, Denmark, Hungary, Poland, Venezuela
Medtronic - MITG

Terminated

Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study

Upper GI Bleeding

Israel
Western University, Canada
London Health Sciences Centre

Completed

Evaluation of Oscillatory Positive Expiratory Pressure (oPEP) in Bronchiectasis and COPD

Bronchiectasis | Chronic Obstructive Pulmonary Disease

Canada
LivaNova

Completed

VAgal Nerve Stimulation: safeGUARDing Heart Failure Patients (VANGUARD)

Heart Failure With Reduced Ejection Fraction

France, Serbia, Norway, Belgium
Baystate Medical Center

Withdrawn

Bariatric Surgery Telemedicine Study

Obesity

United States
W.L.Gore & Associates

Completed

Open Complex Ventral Incisional Hernia Repair Using Biosynthetic Material for Midline Fascial Closure Reinforcement (COBRA)

Ventral Incisional Hernia

United States, Netherlands
University of Mogi das Cruzes

Completed

Changes in Grip Strength by Using Bandage Kinesio Taping

Hand Strength
Aesculap AG

Completed

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

Incisional Hernia Repair

Germany
Boehringer Ingelheim

Completed

Safety and Tolerability of Pharmaton Capsules in Healthy Volunteers

Healthy
Tabriz University

Completed

Coronally Advanced Flap in Combination With Acellular Dermal Matrix and Enamel Matrix Derivatives for Root Coverage

Gingival Recession

Iran, Islamic Republic of
Alejandro Rodriguez Oviedo , MD
BioMérieux; Biocartis

Recruiting

Molecular Early Sepsis Identification Study (MESIS)

Sepsis | Molecular Diagnosis

Spain
MicroPort Orthopedics Inc.

Active, not recruiting

Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing Inserts (AMETHYST)

Joint Disease

Canada, United States, Belgium, Germany, United Kingdom
Hospital Universitario Central de Asturias
Johnson & Johnson

Unknown

Evaluation of Thermocool SF Catheter on the Common Cavo-tricuspid Isthmus Dependent Atrial Flutter Ablation

Atrial Flutter.

Spain
Alcon Research

Completed

DAILIES TOTAL1® Lens Centration in a Japanese Population

Refractive Error | Myopia

Japan
Cook Group Incorporated

Completed

Advance® 18PTX® Balloon Catheter Study

Peripheral Arterial Disease

Germany, Russian Federation
Alcon Research

Completed

Clinical Evaluation of Two Daily Disposable Silicone Hydrogel Contact Lenses

Myopia
Azienda Socio Sanitaria Territoriale degli Spedali...

Completed

The Efficacy of Full Mouth Erythritol Powder Air-Polishing Therapy (FM-EPAPT) Versus Traditional Ultrasonic Debridment (UD): a Randomized Controlled Study. (ERICO)

Gingivitis

Italy
Thorax Centrum Twente

Unknown

DUrable Polymer-based STent CHallenge of Promus ElemEnt Versus ReSolute Integrity (DUTCHPEERS)

Coronary Artery Disease | Angina Pectoris | Acute Coronary Syndrome | Unstable Angina Pectoris | Coronary Stenosis | Coronary Restenosis

Netherlands
University Hospital, Basel, Switzerland
Swiss National Science Foundation

Completed

PROVOCATION Trial - PROphylactic intraVenOus Hydration for Contrast Agent Toxicity PreventION

Kidney Failure, Acute

Switzerland, Italy
Nanfang Hospital of Southern Medical University

Terminated

Safety of Dual Blockage of Rennin-angiotensin System in Patients With Advanced Renal Insufficiency (SDBRAS)

Renal Insufficiency, Chronic

China
Pharmacosmos A/S

Completed

Iron Isomaltoside/Ferric Derisomaltose vs Iron Sucrose for Treatment of Iron Deficiency Anemia in Non-Dialysis-Dependent Chronic Kidney Disease

Chronic Kidney Disease | Iron Deficiency Anemia | Iron Deficiency Anaemia

United States
Merit Medical Systems, Inc.

Not yet recruiting

Observational Study of the Merit HeRO® Graft and Super HeRO® in Patients on Hemodialysis (PReSeRVE-HD)

End Stage Renal Disease | Hemodialysis Access Failure
Avantec Vascular
Bright Research Partners; Yale Cardiovascular Research Group

Recruiting

The Golazo® Peripheral Atherectomy System for a Safe and Effective Atherectomy (GREAT Trial) (GREAT)

Peripheral Arterial Disease

United States
CHU de Reims

Recruiting

Home-based Exercice Therapy for Patients With Intermittent Claudication Using a New Smartphone Application (APAISE)

Intermittent Claudication

France
The Archer-Daniels-Midland Company
Atlantia Food Clinical Trials; Teagasc

Completed

Digestion of Gluten in the Presence of Enzymes (GlutDigest)

Main Focus: Gluten and Starch Digestibility

Ireland
University Hospital, Basel, Switzerland

Completed

Neoveil® Versus TachoSil® for the Treatment of Pulmonary Air Leaks Following Lung Operation

Prolonged Air Leak | Postoperative Air Leak

Switzerland
Children's Hospital Medical Center, Cincinnati
ExThera Medical Corporation

Enrolling by invitation

Registry of Seraph®-100 Microbind® Affinity Blood Filter for COVID-19 Under EUA

COVID-19 | SARS-CoV 2

United States
Actinogen Medical
Avance Clinical

Completed

A Double-Blind, Placebo-Controlled, Dose Ranging Study of Xanamem® in Healthy Elderly Volunteers (XanaMIA-DR)

Mild Cognitive Impairment | Alzheimer's Disease

Australia
WellSpan Health
University of Pennsylvania

Completed

Intraosseous Access in the Emergency Department for Patients With Failed Attempts at Intravenous Access: A Randomized Trial Examining Resource Utilization and Patient Satisfaction

Difficult Peripheral IV Access

United States
Shaperon

Completed

Clinical Trial to Investigate the Efficacy and Safety of NuSepin® in COVID-19 Pneumonia Patients

COVID19 Pneumonia

Romania
Shin Poong Pharmaceutical Co. Ltd.

Completed

Efficacy and Safety for Medicurtain® in Prevention of Adhesion After Endoscopic Sinus Surgery (Pivotal Study)

Sinusitis | Tissue Adhesion, Surgery-Induced

Korea, Republic of
Integra LifeSciences Corporation
Vanderbilt University Medical Center

Withdrawn

A Study to Evaluate the Efficacy of Cytal® Burn Matrix in the Management of Partial-Thickness Burns to the Hand

Partial Thickness Burn of Hand
Wills Eye
Harold P. Koller, MD; Judith B. Lavrich, MD

Unknown

Transcorneal Electrical Stimulation (TES) for the Treatment of Amblyopia

Amblyopia

United States
Medtronic Spine LLC

Withdrawn

Effects of X-STOP® Versus Laminectomy Study (EXELS)

Lumbar Spinal Stenosis
Sanofi Pasteur, a Sanofi Company

Completed

REVAXIS® Versus DT Polio® as a Second Booster in 6 Year-old Children

Tetanus | Diphtheria | Poliomyelitis

France
Asahi Kasei Pharma Corporation

Completed

Collagenase Option for Reduction of Dupuytren's Contracture in Japan (CORD-J)

Dupuytren's Contracture

Japan
W.L.Gore & Associates

Terminated

Study of GORE® BIO-A® Fistula Plug for Use in Anal Fistula Repair

Anal Fistula
Sanofi Pasteur, a Sanofi Company

Completed

Safety and Immunogenicity of DAPTACEL® as 5th Dose in Children 4 to 6 Years Old After 4 Doses of Pentacel™ or DAPTACEL®

Pertussis | Tetanus | Diphtheria

United States
nContact Surgical Inc.

Terminated

Safety and Efficacy Study of The Combined Ablation Procedure To Treat Longstanding Persistent Atrial Fibrillation (CAPstopsLSPAF)

Atrial Fibrillation

United States
NeuroPace

Completed

RNS® System Feasibility Study

Epilepsy

United States
Alcon Research

Completed

Clinical Evaluation of a Daily Disposable Contact Lens in Symptomatic Weekly/Monthly Lens Wearers

Myopia | Dry Eye Syndrome
NeuroPace

Completed

RNS® System Pivotal Study

Epilepsy

United States

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