Found 86 matching trials
Study of Innovative Drug Strategies in Improving Left Ventricular Function After Mitral Repair N/A The goal of this observational study is to compare the safety and effective...
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The Effect of BI 187004 on the Pharmacokinetics of Cytochrome P450 Substrates (Caffeine, Warfarin, Omeprazole, Metoprolol and Midazolam) and a P Glycoprotein Substrate (Digoxin) PHASE1 To assess the influence of BI 187004 on kinetics of cytochrome P450 (CYP) a...
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1307.19.1 Boehringer Ingelheim Investigational Site
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Combined Antihypertensive Therapy and Sexual Dysfunction PHASE4 This randomized,active controlled study aimed to compare the effects on sex...
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The Second Hospital of Lanzhou University
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Pharmacodynamic Effects, Safety and Tolerability of Cilobradine, Compared to Metoprolol Succinate and Placebo in Healthy Volunteers PHASE1 Pharmacodynamic effects on heart rate (HR) at rest and during exercise and ...
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Multiple Locations
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Study to Investigate the Pharmacokinetic Profile PHASE1 A randomized, open-label, single-dose, parallel-arm, Phase 1 study to inves...
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Early Phase Clinical Unit;Klinikum Westend, Haus 31
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Co-Administration of MK-4618 With Antihypertensive Agents (MK-4618-010) PHASE1 This study will evaluate the safety and tolerability of MK-4618 when coadmi...
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Multiple Locations
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Study of Drug Therapy for Pediatric Heart Failure N/A The goal of this observational study is to compare the safety and effective...
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Supramaximal Titrated Inhibition of RAAS in Dilated Cardiomyopathy PHASE4 Dilated cardiomyopathy (DCM) is a poorly understood cause of systolic heart...
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Xijing Hospital, Department of Cardiology
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The Efficacy and Safety of Metoprolol as add-on Treatment to Standard of Care in Preventing Cardiomyopathy in Patients With DMD PHASE3 The study includes 150 patients with DMD diagnosis confirmed by genetic tes...
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University Clinical Centre in Gdańsk, Clinic of Paediatric Cardiology and Congenital Heart Defects
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307B - Safety, Tolerability and Pharmacokinetics Study of TOPROL-XL® in Hypertensive Pediatric Subjects PHASE3 This was a 52-week, multicenter, open-label study to determine the safety, ...
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