Search clinical trials for: DVS SR

Total 80828 results

University Hospital of Limerick

Not yet recruiting

Effect of Environmental Temperature on Vascular Ultrasound Vein Scan Measurements

Critical Limb Ischemia
University Hospital, Lille

Not yet recruiting

Severe Congenital Hemostatic Defects, Cerebral MIcrobleeds and COGnition (HEMICOG)

Cerebral Microbleeds, Congenital Haemophilia, Congenital Von Willebrand Disease
University Hospital of Limerick

Recruiting

The Biomechanical Study of Diseased Human Carotid, Femoral and Abdominal Aortic Tissue

Vascular Diseases

Ireland
Indiana University
Eunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaborators

Recruiting

Variable Intensive Early Walking Post-Stroke - 2 (VIEWS-2) (VIEWS-2)

Stroke

United States
University Hospital of Limerick

Not yet recruiting

Vascular Surgery Admissions in a Tertiary Care Hospital in the Mid-West: A 12 Month Profile.

Vascular Diseases
University Hospital of Limerick

Not yet recruiting

Prevalence of May-Thurner Syndrome in 1st-degree Relatives of Symptomatic Patients (MTS)

May-Thurner Syndrome
University of Texas at Austin

Recruiting

Non-invasive BCI-controlled Assistive Devices

Stroke | Multiple Sclerosis | Healthy | Muscular Diseases | Movement Disorders | Motor Neuron Disease | Traumatic Brain Injury | Spinal Cord Injuries | Motor Disorders

United States
Umeå University
Karolinska Institutet; Uppsala University; The Swedish Research Council; Göteborg... and other collaborators

Recruiting

Rehabkompassen® - a Patient-centered Digital Follow-up Tool in the Post-stroke Continuum of Care

Stroke

Sweden
Direction Centrale du Service de Santé des Armées

Recruiting

Management by Hyperbaric Oxygen Therapy of Patients With Hypoxaemic Pneumonia With SARS-CoV-2 (COVID-19) (OHB10cov)

Covid-19

France
Duke University
Eunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaborators

Recruiting

Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS) (POPS or POP02)

Heart Failure | Pain | Pneumonia | Hypertension | Edema | Hemophilia | Insomnia | Pulmonary Arterial Hypertension | Coagulation Disorder | Asthma in Children | Down Syndrome | Attention Deficit Hyperactivity Disorder | Bronchopulmonary Dysplasia | Hypokalemia | Hyperphosphatemia | Primary Hyperaldosteronism | Adrenal Insufficiency and other conditions

United States, Canada
University Hospital, Grenoble

Recruiting

Angioplasty-stenting vs Optimal Medical Treatment on Post-thrombotic Syndrome Reduction (EndoPTS)

Post Thrombotic Syndrome

France
ZeaVision, LLC

Recruiting

Combined Effects of Diabetes Self-Management Education and Nutritional Supplementation on Visual Function and Retinopathy

Diabetes Mellitus | Diabetic Retinopathy

United States
ZeaVision, LLC
Western University of Health Sciences; Northeastern State University; Diopsys...

Recruiting

Diabetic Retinopathy Functional Evaluation Study: Monitoring Carotenoid Vitamins Treatment Using ERG

Diabetes | Diabetic Retinopathy

United States
University Hospital of Limerick
University of Limerick

Recruiting

The Mechanical Characterisation of Human Saphenous and Popliteal Vein

Peripheral Vascular Diseases

Ireland
Sanford Health
National Ataxia Foundation; Beyond Batten Disease Foundation; Pitt Hopkins Research... and other collaborators

Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford (CoRDS)

Mitochondrial Diseases | Retinitis Pigmentosa | Myasthenia Gravis | Eosinophilic Gastroenteritis | Multiple System Atrophy | Leiomyosarcoma | Leukodystrophy | Anal Fistula | Spinocerebellar Ataxia Type 3 | Friedreich Ataxia | Kennedy Disease | Lyme Disease | Hemophagocytic Lymphohistiocytosis | Spinocerebellar Ataxia... and other conditions

United States, Australia
University Hospital of Limerick

Completed

Cost Analysis of Vascular Surgical Techniques

Critical Limb Ischemia

Ireland
University Hospital of Limerick
University of Limerick

Terminated

The Role of Unsteady Wall Shears Stress Stimuli on Human Umbilical Vein Endothelial Cells Harvested From Umbilical Cords (HUVEC)

Vascular Diseases

Ireland
Centre Cardiologique du Nord
University of Bristol; Universita degli Studi di Genova; Campus Bio-Medico University and other collaborators

Enrolling by invitation

Infective Endocarditis Surgery Using Conventional Prosthetic Valves Versus Cryopreserved Aortic Homograft (IESCOPHO)

Heart Failure | Infective Endocarditis

France
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women

Depressive Disorder | Depression | Depressive Disorder, Major

Colombia, Mexico, United States, Peru, Chile, Argentina
University Hospital of Limerick

Completed

Differential Effects of Bacteria Colonising Venous Leg Ulcers on Pain and Healing Rates

Venous Leg Ulcer

Ireland
Wyeth is now a wholly owned subsidiary of Pfizer

Terminated

Study Evaluating the Long-Term Safety of Desvenlafaxine Succinate Sustained-Release (DVS SR) in Subjects With Pain Associated With Diabetic Peripheral Neuropathy

Diabetic Neuropathy, Painful
Assistance Publique - Hôpitaux de Paris

Completed

Cost-utility Analysis of Fenestrated Aortic Stents Versus Open Surgery for the Treatment of Complex Abdominal Aortic Aneurysms (ORFEVAR)

Complex Abdominal Aortic Aneurysm, ie. Juxtarenal or Suprarenal Aortic Aneurysms, Treated by Fenestrated Endovascular Aortic Aneurysm Repair or Open Repair

France
University Hospital of Limerick

Completed

Arterio-Venous Fistula Audit. Successful Utilisation Rates of Arterio-Venous Fistulae for Haemodialysis at University Hospital Limerick

Arterio-venous Fistula

Ireland
University Hospital of Limerick
University of Limerick

Completed

Invasive Arterio-Venous Fistula Blood Pressure Monitoring & Fluid Dynamics Study

Arterio-venous Fistula

Ireland
University of Pittsburgh

Withdrawn

Short Atrioventricular Delay Pacing (SAVD)

Chronically (i.e. Implanted for at Least Six Months) Dual-chamber Pacemaker | Stable Cardiac Status (i.e. no Hospitalizations or Cardiac Medication Changes Within 3 Months)

United States
Riphah International University

Completed

Chair Rise and Step Ups on Cardiopulmonary Parameters Among Preserved Ejection Heart Failure Patients

Heart Failure

Pakistan
Hospices Civils de Lyon

Withdrawn

Low Health Literacy Prevalence's Study in Patients With Chronic Cardiovascular Disease (LIT-S)

Cardiovascular Diseases
Viz.ai, Inc.
Nico Corporation

Enrolling by invitation

AI ENRICH - AI Detection of ICH

Intracerebral Hemorrhage

United States
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Evaluating Desvenlafaxine Succinate Sustained-Release Tablets (DVS SR) In The Treatment Of Child and Adolescent Outpatients With Major Depressive Disorder

Depressive Disorder, Major Depressive Disorder

United States
National Taiwan University Hospital

Unknown

Comparison of Different Drugs on Ocular Surface Disease in Glaucoma Patients: a Prospective Randomised Study

Glaucoma; Ocular Disorders (I.E. Caused by Ocular Disorders)

Taiwan
Providence Little Company of Mary-Torrance
Viz.ai, Inc.

Unknown

Automated Detection and Triage of Large Vessel Occlusions Using Artificial Intelligence for Early and Rapid Treatment (ALERT) (ALERT)

Stroke Workflow and Clinical Outcome Parameters

United States
Pfizer

Completed

A Study Of DVS SR In Treatment Of Children And Adolescent Outpatients With MDD

Major Depressive Disorder

United States, Mexico
Pfizer

Completed

A 6-Month Extension Study To The B2061032 Study To Evaluate The Safety, Tolerability, And Efficacy Of DVS SR In The Treatment Of Child And Adolescent Outpatients With MDD

Major Depressive Disorder

United States, Chile
Pfizer

Completed

A Study Of DVS SR In Treatment Of Children And Adolescent Outpatients With MDD

Major Depressive Disorder

United States, Chile, Mexico
Pfizer

Completed

A 6-Month Open-Label Extension Study to the B2061014 Study to Evaluate the Safety, Tolerability and Efficacy of DVS SR in the Treatment of Children and Adolescents With MDD

Major Depressive Disorder

United States, Mexico
Assistance Publique - Hôpitaux de Paris
European Union

Unknown

Metagenomics and Integrative Systems Medicine of Cardiometabolic Diseases (METACARDIS)

Cardiometabolic Disease

Denmark, France, Germany
Pfizer

Completed

Study Evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) in Adult Outpatients With Major Depressive Disorder (MDD)

Major Depressive Disorder

United States
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Paroxetine-referenced Study Evaluating Three Doses of DVS SR in Outpatients With MDD

Depressive Disorder, Major

Korea, Republic of, India, China, Taiwan
Wyeth is now a wholly owned subsidiary of Pfizer

Terminated

A Study Evaluating Desvenlafaxine Sustained Release (DVS SR) in Adult Female Outpatients With Fibromyalgia

Fibromyalgia

United States
Lagos State University

Completed

The Efficacy of Jobelyn (Sorghum Bicolor Extract)in the Treatment of Sickle Cell Anemia

Sickle Cell Anemia

Nigeria
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) Versus Placebo in Peri- and Postmenopausal Women

Depressive Disorder | Depression | Depressive Disorder, Major

United States
Pfizer

Completed

Study Evaluating Desvenlafaxine Succinate Sustained-Release (DVS SR) In The Treatment Of Peri- And Postmenopausal Women With Major Depressive Disorder (DVS 3364)

Major Depressive Disorder

United States
Pfizer

Completed

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) In The Treatment Of Major Depressive Disorder

Depressive Disorder, Major

United States
Pfizer

Completed

Study Comparing Discontinuation Symptoms Of DVS SR In Subjects With Major Depressive Disorder (MDD)

Major Depressive Disorder
Pfizer

Completed

Phase 1 Study To Test the Bioequivalence Between Two 25 mg Tablets vs. One 50 mg Tablet Under Fast/Fed Condition and Evaluate Food Effect of Desvenlafaxine Succinate Sustained Release (DVS SR)

Depression - Major Depressive Disorder

Belgium
Pfizer

Completed

Open Label Drug Interaction Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) 100mg On The Pharmacokinetics Of Aripiprazole When Coadministered To Healthy Subjects

Pharmacokinetics | Cytochrome P-450 CYP2D6 | CYP3A4 Protein, Human

United States
Pfizer

Completed

Open-Label Drug Interaction Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) 100mg On The Pharmacokinetics Of Tamoxifen When Coadministered To Healthy Post-Menopausal Female Subjects

Pharmacokinetics

United States
Pfizer

Completed

The Effect Of Dose Titration And Dose Tapering On The Tolerability Of DVS SR In Women With Vasomotor Symptoms

Vasomotor Symptoms

Canada, United States
Wyeth is now a wholly owned subsidiary of Pfizer

Terminated

Study Evaluating Desvenlafaxine Succinate Sustained-release (DVS SR) in Adult Outpatients With Pain Associated With Diabetic Peripheral Neuropathy

Pain | Diabetic Neuropathies

United States
Pfizer

Completed

Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women

Vasomotor Symptoms

Canada, United States

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