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Development and Feasibility Testing of a Group-based PFMT Programme for Antenatal Women in Nanjing City in China NA The main objective is to co-design and assess the practicality of group-bas...
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Nanjing Maternity and Child Health Care Hospital
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STRATA: Safe Testing of Risk for AsymptomaTic MicrohematuriA NA To evaluate the clinical utility associated with the integration of Cxbladd...
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Institute of Urology, USC Norris Comprehensive Cancer Center
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Efficacy, Tolerability and Safety of LAS41004 Formulations in a Psoriasis Plaque Test PHASE1 Clinical investigation of anti-psoriatic efficacy and atrophy...
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Bioequivalence Study Comparing A New 80 Mg Atorvastatin Tablet To A 80 Mg Atorvastatin Commercial Tablet PHASE4 To determine whether new 80 mg atorvastatin tablets are bioequivalent to 80...
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Pfizer Investigational Site
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Strengthening, Guidance, Health, Empowerment NA The goal of this interventional study is to describe the care pathway follo...
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ROSELA _ Médecins du Monde
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Study Comparing Blood Levels of Fatty Acids After Consuming Two Forms of Cod Liver Oil NA This study is designed to compare the incremental area under the curve from...
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GSK Investigational Site
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TMS-EEG for Cortical Excitability NA This research study is being done to look at the safety and diagnostic bene...
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Multiple Locations
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SCH 52365 Phase II Clinical Study: A Study on the Efficacy and Safety of Monotherapy With SCH 52365 in Patients With First Relapsed Anaplastic Astrocytoma (Study P03745) PHASE2 The primary purpose of the study is to evaluate the efficacy (overall respo...
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Multiple Locations
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Human Pharmacology Study (Keppra Dry Syrup Bioequivalence Study) PHASE1 To demonstrate the bioequivalence of a Levetiracetam dry syrup (50% (500mg/...
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Multiple Locations
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A Study of On-treatment ctDNA Changes in Chemo-refractory Colorectal Cancer Patients NA COPERNIC is an international, multicentre, single-arm study. Chemo-refracto...
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Institut Jules Bordet
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