Search clinical trials for: metoprolol succinate and nebivolol

Total 703 results

Boehringer Ingelheim

Terminated

Telmisartan Effectiveness on Left Ventricular Mass Reduction (TELMAR) as Assessed by MRI, in Patients With Mild to Moderate Hypertension

Hypertension
IPCA Laboratories Ltd.

Completed

Bioequivalence Study of Metoprolol Succinate Extended Release Tablets 200 mg Under Fed Conditions

Fed

India
Forest Laboratories

Completed

A Study of the Effect of Nebivolol to Evaluate Its Vasodilatory Effects in Hypertensive Patients

Hypertension

United States
IPCA Laboratories Ltd.

Completed

Bioequivalence Study of Metoprolol Succinate Extended Release Tablets 200 mg Under Fasting Conditions

Fasting

India
University of Abuja
Micronova Pharmaceuticals Ind Ltd

Completed

To Determine the Effect of Nebivolol on Office Blood Pressure of Blacks Residing in Nigeria (Nevibolol)

Hypertension

Nigeria
University of Pennsylvania
Julio Chirinos, MD, PhD; Raymond Townsend, MD

Recruiting

BLOCKade of Calcium Channels and Beta Adrenergic Receptors for the Treatment of Hypertension in HFpEF (BLOCK HFpEF)

Hypertension | Heart Failure With Preserved Ejection Fraction

United States
Huashan Hospital

Completed

the Efficacy and Safety of Vitamin C for Iron Supplementation in Adult IDA Patients

Anemia, Iron-Deficiency

China
Boehringer Ingelheim

Completed

Pharmacodynamic Effects, Safety and Tolerability of Cilobradine, Compared to Metoprolol Succinate and Placebo in Healthy Volunteers

Healthy
University of Vermont

Recruiting

Atrial Fibrillation: Chronic Beta-blocker Use Versus As-needed Rate Control Guided by Implantable Cardiac Monitor

Atrial Fibrillation | Diastolic Dysfunction | HFpEF - Heart Failure With Preserved Ejection Fraction

United States
Astellas Pharma Inc

Completed

Relative Bioavailability Study of Solifenacin Succinate Liquid Suspension (Fed and Fasting) Versus VESIcare Tablet (Fasting) in Healthy Volunteers

Healthy Volunteers | Pharmacokinetics of Solifenacin Succinate | Bioavailability of Solifenacin Succinate

United States
Ain Shams University

Recruiting

Evaluating the Outcome of Cardio Selective beta1- Blockers Use in Patients With Copd

Copd

Egypt
Astellas Pharma Europe B.V.

Completed

A Clinical Study to Investigate How Solifenacin Fluid is Taken up, How Long it Stays in the Body and How Effective and Safe it is in Treating Children Aged From 6 Months to Less Than 5 Years With Symptoms of Neurogenic Detrusor Overactivity (NDO)

Pediatric | Neurogenic Detrusor Overactivity

United States, Belgium, Korea, Republic of, Philippines, Poland, United Kingdom
GlaxoSmithKline

Completed

Use of Beta-blockers and Risk of New Onset Diabetes

Hypertension
Astellas Pharma Europe B.V.

Completed

A Study to Investigate How Safe and Effective Solifenacin Solution is in Treating Children/Adolescents With Symptoms of Overactive Bladder (OAB) Who Completed Study 905-CL-076 (LEOPARD)

Urinary Bladder, Overactive

Belgium, United States, Brazil, Canada, Denmark, Former Serbia and Montenegro, Korea, Republic of, Mexico, Norway, Philippines, Poland, South Africa, Sweden, Turkey, Ukraine, United Kingdom
Center Eugene Marquis

Terminated

Solifenacin Succinate for Treatment of Urinary Toxicity Occurring During Radiotherapy of Prostatic Cancer (VesiCaP)

Overactive Bladder

France
Astellas Pharma Inc

Completed

Single-dose Study to Assess Pharmacokinetics of Solifenacin Succinate Suspension in Children and Adolescents

Urinary Bladder, Overactive

Sweden, United Kingdom, Belgium, Denmark
AstraZeneca

Completed

Efficacy and Safety of Metoprolol Succinate Prolonged-Release Tablet in Patients With Mild to Moderate Hypertension

Hypertension
Odense University Hospital

Not yet recruiting

Are Carvedilol and Metoprolol Succinate Comparable Treatments in Heart Failure Patients With Reduced Ejection Fraction (CROWD-COMPARE)

Chronic Heart Failure

Denmark
Forest Laboratories

Completed

Efficacy and Safety Study to Evaluate Combination Therapy With Nebivolol and Lisinopril vs. Placebo and Monotherapy in Patients With Stage 2 Diastolic Hypertension

Stage 2 Diastolic Hypertension

United States, Puerto Rico
Jack Rubinstein
Forest Laboratories

Terminated

An Advanced Echocardiographic Evaluation of Nebivolol

Hypertension

United States
Radboud University Medical Center

Completed

Immunization With Different Doses of Plasmodium Falciparum Sporozoites Under Chloroquine Prophylaxis (ZonMw1)

Plasmodium Falciparum Malaria

Netherlands
Sanofi

Completed

An Eight-Week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression

Depressive Disorder

France, Canada, Germany, Portugal, Czech Republic, Mexico, Croatia, Chile
VA Office of Research and Development

Recruiting

CSP #2026 - Beta Blocker Dialyzability on Cardiovascular Outcomes (BRAVO)

End-Stage Renal Disease | End-Stage Kidney Disease

United States
Creighton University

Withdrawn

Impact of Nebivolol on Central Aortic Pressure

Central Aortic Pressure

United States
I.M. Sechenov First Moscow State Medical University

Completed

A Pooled Analysis of the Data From Two Studies of Ammonium Succinate for Menopausal Symptoms

Menopause Related Conditions

Russian Federation
Astellas Pharma Inc

Completed

A Study in Healthy Volunteers Comparing Two Different Liquid Formulations of Solifenacin With Each Other and With the Tablet Formulation

Healthy Volunteers | Pharmacokinetics of Solifenacin Succinate

United States
Forest Laboratories

Completed

A Study on the Long-term Efficacy of Nebivolol After Withdrawal of Therapy

Hypertension

United States
Zhejiang Provincial Center for Disease Control...
China National Biotec Group Company Limited

Not yet recruiting

Immunogenicity and Safety of DTaP or DT Vaccine in 6 Year Old Children ( DTaP/DT ) (DTaP/DT)

Vaccine Reaction

China
AstraZeneca

Completed

Metoprolol in Acute Myocardial Infarction. A PK/PD Study

Acute Myocardial Infarction
VA Greater Los Angeles Healthcare System
AstraZeneca

Completed

Tolerability of Metoprolol-Succinate-ER and Carvedilol in COPD

Pulmonary Disease, Chronic Obstructive | Asthma | Adverse Effect of Beta-adrenoreceptor Antagonists

United States
Sanofi

Completed

An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression

Depressive Disorder

Canada, Germany, Portugal, Estonia, Mexico, Croatia, Chile, Czechia
Sanofi

Completed

A Fifty-two-week Study to Evaluate the Safety of Saredutant in Adult and Elderly Patients With Depression

Depressive Disorder

United States
Sanofi

Completed

An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression

Depressive Disorder

United States
Sanofi

Completed

An Eight-week Study to Evaluate the Efficacy and Safety of Saredutant in Patients With Depression

Depressive Disorder

United States
Forest Laboratories

Unknown

Economic Impact of Switching From Metoprolol to Nebivolol for Hypertension Treatment

Hypertension

United States
Vanderbilt University

Completed

Comparative Effect of Nebivolol vs. Metoprolol on Insulin Sensitivity and Fibrinolytic Balance in Metabolic Syndrome

Metabolic Syndrome

United States
Beijing Tiantan Hospital

Unknown

Efficacy and Safety of Ferrous Iron on the Prevention of Vascular Cognitive Impairment Among Patients With Cerebral Infarction/TIA (FAVORITE) (FAVORITE)

Iron-deficiency | Cerebral Infarction | Dementia, Vascular | TIA | Vascular Cognitive Impairment

China
POLYSAN Scientific & Technological Pharmaceutical...
Atlant Clinical Ltd.

Completed

Meglimine Sodium Succinate for Correction of Metabolic Acidosis in Critically Ill Patients

Metabolic Acidosis

Russian Federation
Brigham and Women's Hospital
University of California, Los Angeles; POM Wonderful LLC

Completed

Impact of Antioxidant Juice Intake on Brain Injury and Placental Pathology in Infants With Intrauterine Growth Restriction (IUGR)

Intrauterine Growth Restriction

United States
Menarini International Operations Luxembourg SA

Completed

Effectiveness and Safety of Combination of Nebivolol and Zofenopril in Hypertensive patIents Versus Each Monotherapy (Masaccio)

Hypertension

Italy
University of Colorado, Denver
National Institute of General Medical Sciences (NIGMS)

Terminated

Pharmacogenetic Prediction of Metoprolol Effectiveness

Hypertension

United States
GlaxoSmithKline

Completed

COREG MR Versus TOPROL-XL On The Lipid Profile Of Normolipidemic Or Mildly Dyslipidemic Patients With Hypertension

Hypertension

United States, Canada, Puerto Rico
Jiangsu HengRui Medicine Co., Ltd.

Unknown

A Phase Ⅲ Study of Extended-Release Carvedilol Sulfate for the Treatment of Heart Failure

Heart Failure

China
Bright Future Pharmaceuticals Factory O/B Bright...
Chinese University of Hong Kong

Unknown

Clinical Bioequivalence Study on Two Metoprolol Tablet 100mg Formulations

Healthy
Betaliq, Inc.
Trial Runners, LLC; Summit Analytical, LLC

Completed

Nebivolol 0.5, 1.0, or Timolol 0.5 Suspension Compared to Timolol 0.5 Solution to Treat Glaucoma/Ocular Hypertension

Ocular Hypertension | Open-Angle Glaucoma

United States
AstraZeneca
St. John's Research Institute

Completed

A Study to Compare the Efficacy, Safety and Tolerability of Selomax With Its Individual Components (MARS)

Primary Hypertension

India
Pharmasoft

Completed

MEXIDOL® Sequential Therapy of Patients With Acute Cerebral Failure (MIR)

Ischemic Stroke, Acute

Russian Federation, Kazakhstan, Uzbekistan
Seoul National University Hospital
Pfizer; Seoul National University Bundang Hospital; Korea Cancer Center Hospital

Terminated

Desvenlafaxine for Treatment of Hot Flashes in Women With Breast Cancer Taking Tamoxifen

Breast Neoplasms | Hot Flashes

Korea, Republic of
Weill Medical College of Cornell University
Forest Laboratories

Completed

Nebivolol Versus Metoprolol: Comparative Effects on Fatigue and Quality of Life

Hypertension

United States
University of Florida
Forest Laboratories

Completed

Nebivolol Effect on Nitric Oxide Levels, Blood Pressure, and Renal Function in Kidney Transplant Patients

Hypertension

United States

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