spironolactone + furosemide
Drugspironolactone 25mg/day, 16 weeks and furosemide 20mg/day, 16 weeks
NCT Number: NCT00663195
The purpose of this study is to evaluate the effects of spironolactone on circulating MMP levels and insulin resistance in patients with chronic heart failure.
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Interventional
Phase 4
Myocardial fibrosis is observed in failing hearts. MMPs are considered markers of fibrosis. Recently, circulating MMPs can be measured and are elevated in patients with chronic heart failure (CHF). It has been reported that spironolactone improves myocardial fibrosis in CHF animal models. Therefore, the purpose of this study is to evaluate the effects of spironolactone on circulating MMP levels in patients with chronic heart failure.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
spironolactone 25mg/day, 16 weeks and furosemide 20mg/day, 16 weeks
Time frame: 16 weeks
Tottori University Hospital
Other
Effects of Spironolactone on Circulating MMPs in Patients With Chronic Heart Failure
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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