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Clinical Trial Details

Trial ID: L2261
Source ID: NCT01181830
Associated Drug: Magnesium Pidolate
Title: Effect of Magnesium Administration in Subjects With Family History of Diabetes or Metabolic Syndrome
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Family History of Metabolic Syndrome|Family History of Diabetes
Interventions: DRUG: magnesium pidolate|DRUG: placebo
Outcome Measures: Primary: Blood pressure, Blood pressure measured in the lying and standing position (average of three measurements);, 8 weeks | Secondary: other features of metabolic syndrome, especially plasma lipids and HOMA index, 8 weeks|endothelial function, endothelial function as measured non-invasively by ultrasound using the "Flow Mediated Dilatation" (FMD) technique, 8 weeks|arterial stiffness, systemic and local arterial stiffness measured by digital photoplethysmography and by carotid ultrasound, 8 weeks|Inflammation, Markers of inflammation such as C reactive protein, 8 weeks
Sponsor/Collaborators: Sponsor: Universita di Verona
Gender: ALL
Age: ADULT
Phases: PHASE4
Enrollment: 14
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2010-02
Completion Date: 2012-12
Results First Posted:
Last Update Posted: 2013-10-16
Locations: Azienda Ospedaliera Universitaria Integrata - Division of Internal Medicine C, Verona, VR, 37134, Italy
URL: https://clinicaltrials.gov/show/NCT01181830