Search clinical trials for: 24-006

Total 4733 results

Sanofi Pasteur, a Sanofi Company

Completed

Study of a Booster Dose of IMOJEV® One Year After Primary Immunization in Healthy Children in South Korea

Japanese Encephalitis

Korea, Republic of
Seqirus
Novartis Vaccines

Completed

Safety and Immunogenicity of Two Doses of aH5N1 Vaccine in Adult and Elderly Subjects With and Without Underlying Medical Conditions

Influenza, Human

Germany
Pfizer

Completed

Evaluation of Risk Minimization, Assessment and Outcomes in Patients With Chronic Pain Taking Avinza (ACCESS 2008)

Pain

United States, Puerto Rico
Vaxcyte, Inc.

Completed

Safety, Tolerability, and Immunogenicity Study of a 24-Valent Pneumococcal Conjugate Vaccine (VAX-24) in Older Adults

Pneumococcal Vaccines

United States
Regeneron Pharmaceuticals
Syneos Health

Withdrawn

Study of the Safety and Effectiveness of Rilonacept (IL-1 Trap) Administered Subcutaneously in Subjects With Non Dialysis-Dependent Chronic Kidney Disease (NDD-CKD) and Anemia

Anemia | Chronic Kidney Disease

United States
Heidelberg University
Wala GmbH

Completed

Treating Climacteric Symptoms With a Complex Homeopathic Remedy

Depression | Anxiety Disorders | Menopause

Germany
Modra Pharmaceuticals

Withdrawn

Absorption and Excretion of Oral Docetaxel

Solid Tumor, Adult

Netherlands
Kaiser Permanente
Patient-Centered Outcomes Research Institute

Completed

Blood Pressure Checks for Diagnosing Hypertension (BP-CHECK)

Blood Pressure

United States
The University of Hong Kong

Terminated

A Pilot Randomized Controlled Trial to Reduce Salt Intake Among Hypertensive Young Adults in Hong Kong

Hypertension

China
Europainclinics z.ú.
University Hospital Bratislava; Slovak Academy of Sciences; R-CLINIC s.r.o.; Faculty...

Recruiting

EuroPainClinicsStudy X (EPCS X)

Back Pain

Slovakia
Global Alliance for TB Drug Development

Completed

Shortening Treatment by Advancing Novel Drugs (STAND)

Tuberculosis, Pulmonary, Drug Sensitive | Tuberculosis, Pulmonary, Multi Drug-resistant

South Africa, Zambia, Georgia, Philippines, Kenya, Malaysia, Tanzania, Uganda
Sensimed AG

Completed

Relationship Between 24-hour IOP Pattern and the 24-hour Blood Pressure Pattern in Patients With POAG

Primary Open Angle Glaucoma | Normal Tension Glaucoma

Poland
Pirogov Russian National Research Medical University

Recruiting

Elastic Compression Stockings and Varicose Veins Recurrence (ECOS-VVR)

Varicose Veins | Chronic Venous Insufficiency

Russian Federation
Duke University
PDI Healthcare Inc.

Completed

Measuring the Impact of an Enhanced Strategy for Daily Disinfection in Acute Care Hospital Rooms

Disinfection

United States
Assistance Publique - Hôpitaux de Paris
Institut National de la Santé Et de la Recherche Médicale, France; Institut... and other collaborators

Completed

Ontogeny of MAIT Cells in Neonates and Hematopoietic Stem Cell Transplant Recipients (NEOMAIT)

Term and Preterm Neonates (24-41 Weeks Gestational Age) | Hematopoietic Stem Cell Transplant Recipient Children

France
Sheba Medical Center

Unknown

Neurodevelopmental Outcomes of Preterm Infants Treated for Pain Management With Repeated Doses of Sucrose 24%

Development

Israel
Anil Nigam

Unknown

Effect of High-Intensity Interval Training Compared to Hydrochlorothiazide on Ambulatory Blood Pressure (DIISCCO)

Hypertension,Essential | Exercise Activity

Canada
Kidney Cancer Research Bureau

Unknown

Intrapleural Instillation of the Nivolumab in Cancer Patients With Pleural Effusion.

Non-small Cell Lung Cancer Metastatic | Pleural Effusion, Malignant | Renal Cell Cancer Metastatic

Russian Federation
AnaptysBio, Inc.

Completed

Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With GPP (GEMINI1)

Generalized Pustular Psoriasis

United States, Australia, Georgia, Germany, Korea, Republic of, Malaysia, Morocco, Poland, Romania, Spain, Taiwan, Thailand, Tunisia, Turkey, Slovakia
M.D. Anderson Cancer Center
Active Biotech AB

Not yet recruiting

Open Label Phase 2 Study of Tasquinimod in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera Myelofibrosis (Post-PV MF), or Post-Essential Thrombocytosis Myelofibrosis (Post-ET MF)

Primary Myelofibrosis | Post-polycythemia Vera Myelofibrosis | Post-Essential Thrombocytosis Myelofibrosis

United States
University of Padova

Completed

Assessment of Physical Performance After Oral Supplementation of Magnesium in a Sample of Old Women in Good Health (Magnesium)

Age Related Muscle Loss

Italy
Lady Hardinge Medical College

Completed

Sucrose to Reduce Pain During Initiation of Venipuncture in Extremely Low Birth Weight Babies

Pain | Neonate | ELBW
University of Oxford
Imperial College London; KEMRI-Wellcome Trust Collaborative Research Program; University of Nairobi and other collaborators

Active, not recruiting

A Study to Test Three Experimental HIV Vaccines in Healthy Adults. (HIV-CORE 006)

HIV-1-infection

Kenya, Uganda, Zambia
John Mascarenhas
National Cancer Institute (NCI); Novartis; Incyte Corporation; Myeloproliferative...

Terminated

Ruxolitinib Prior to Transplant in Patients With Myelofibrosis

Primary Myelofibrosis | Post Essential Thrombocythemia Myelofibrosis | Post Polycythemia Vera Myelofibrosis

United States, Canada, United Kingdom
Saint Thomas Hospital, Panama

Completed

Comparison of Urine Protein/Creatinine Ratio With 24-hour Urine Protein Excretion in Woman With Hypertensive Disorders

Hypertension, Pregnancy-Induced

Panama
Istituto Auxologico Italiano

Completed

Effect of Pharmacological Interventions on Systolic Blood Pressure Drops (SynABPM 2 Proof-of-concept) (SynABPM)

Syncope | Orthostatic Hypotension | Syncope, Vasovagal | Ambulatory Blood Pressure Monitoring | Antihypertensive Drugs

Italy
Karadeniz Technical University

Completed

The Effect of Newborn's First Bath Time on Physiological Variables

Baths

Turkey
Sirion Therapeutics, Inc.

Completed

Study of Cyclosporine in the Treatment of Dry Eye Syndrome (ST-603-006)

Dry Eye Syndromes

United States
Sanofi

Completed

Postmarketing Surveillance Study for Quadrivalent Influenza Vaccine (VaxigripTetra®) in Subjects Aged 6 to 35 Months

Influenza

Korea, Republic of
UCB Pharma

Completed

Rotigotine Versus Placebo As Double Blind Study To Evaluate The Efficacy In Early Stage Idiopathic Parkinson's Disease Patients

IDIOPATHIC PARKINSON'S DISEASE

China
University of Pecs

Recruiting

A Multidimensional Study of Premenstrual Syndrome and Body Image

Sleep | Body Image | Physical Inactivity | Premenstrual Syndrome

Hungary
Taipei Medical University Shuang Ho Hospital

Completed

Effect of Ureteral Stents Length and Location on Related Symptom

Lower Urinary Tract Symptoms | Overactive Bladder Syndrome

Taiwan
Boehringer Ingelheim

Completed

Efficacy and Safety of Talsaclidine in Patients With Mild to Moderate Dementia of Alzheimer Type

Alzheimer Disease
Johnson & Johnson Pharmaceutical Research & Development...

Completed

A Study of the Pharmacokinetics, Safety and Tolerability of Topiramate in Infants (Age 1-24 Months) With Refractory Partial-onset Seizures

Seizures
Kuopio University Hospital

Completed

Atrial Fibrillation Detection: 24 Hour Study (AFIB24h)

Stroke | Arrhythmia Atrial

Finland
The Cooper Health System

Completed

Betamethasone Dosing Interval - 12 or 24 Hours?

Preterm Delivery

United States
Julie Dawson
Kebomed UK

Completed

Safety and Efficacy of PVDF (DynaMesh®-SIS Soft) Retropubic Midurethral Slings in Stress Urinary Incontinence in Women

Urinary Stress Incontinence | Urinary Incontinence,Stress

Germany, United Kingdom
Amsterdam UMC, location VUmc
Syddansk Universitet, Denmark; Stichting Alexander (the Netherlands); Aalborg... and other collaborators

Enrolling by invitation

YoPA - A Youth-centred Participatory Action (YoPA)

Physical Activity | Sleep | Health Promotion

Denmark, Netherlands, Nigeria, South Africa
Asian Institute of Gastroenterology, India

Recruiting

Urgent (<24 Hours) Versus Early (24 to 48 Hours) ERCP for Patients With Mild and Moderate Acute Cholangitis

Acute Cholangitis

India
Johns Hopkins University

Recruiting

Evaluation of Efficacy and Comfort: A Trial on the Incrediwear Back Brace in Patients With Chronic Lower Back Pain

Back Pain | Low Back Pain

United States
Chiesi Farmaceutici S.p.A.

Completed

Study to Evaluate Efficacy/Safety of 4 Doses of CHF5259 Via Dry Powder Inhaler (DPI) in Patients With COPD (GlycoNEXT)

Chronic Obstructive Pulmonary Disease (COPD)

Czechia, Germany, Hungary, Romania
UCB Pharma

Terminated

Effect of Rotigotine on Motor Symptoms in Patients With Advanced Parkinson's Disease (PD) With Motor Fluctuations and Symptoms of Gastrointestinal Dysfunction (ROADMAP)

Advanced Parkinson's Disease

United States
Aga Khan University

Completed

Spot Urine Oxalate to Creatinine Ratio and 24 Hours Urinary Oxalate

Urolithiasis | Hyperoxaluria

Pakistan
University Hospital, Tours

Completed

Lymphangioleiomyomatosis, a Study on Cathepsin K (LAM-CAK)

Tuberous Sclerosis Complex | Lymphangioleiomyomatosis

France
Aelix Therapeutics

Completed

Safety and Immunogenicity Study of DNA.HTI, MVA.HTI and ChAdOx1.HTI in HIV-1-positive Patients (AELIX-002)

HIV

Spain
Cancer Trials Ireland

Completed

TC Avastin. ICORG 08-10, V6

Breast Cancer

Ireland, Denmark
Consorci d'Atenció Primària de Salut de l'Eixample
Instituto de Salud Carlos III

Completed

Validity of 1BPM for Diagnosis of Hypertension

Hypertension

Spain
Novartis

Completed

Effects of Rivastigmine Patch on Activities of Daily Living and Cognition in Patients With Severe Dementia of the Alzheimer's Type (ACTION) (Study Protocol CENA713DUS44, NCT00948766) and a 24 Week Open-label Extension to Study CENA713DUS44 (ACTION)

Alzheimer's Disease

United States, Puerto Rico
Charite University, Berlin, Germany
German Federal Ministry of Education and Research

Completed

3 Tesla (3T) Stroke Medical Radiologic Technology (MRT) for Examining Mismatch in 1000+ (1000Plus)

Transient Ischemic Attack | Acute Stroke

Germany
University Hospital, Gentofte, Copenhagen

Completed

Incretin Effect in PCOS Women

Polycystic Ovary Syndrome

Denmark

Search clinical trials for: 24-006

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