Medical University of Ohio
Toledo, Ohio, 43614, United States
NCT Number: NCT00860340
To determine if the beneficial effect of spironolactone in patients with congestive heart failure is in part due to its intrinsic inotropic action.
Randomized, two group placebo controlled, single blind study.
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Notify Me21 year–80 year
All sexes
Interventional
Not applicable
Toledo, Ohio, 43614, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
100 mg tablet of Spironolactone (Aldactone) by mouth with half a glass of water.
Time frame: 3 measurements 15 minutes apart before drug and 15 minutes for 2 hours after drug
Time frame: This will be taken before drug, two hours after and the following day
University of Toledo Health Science Campus
Other
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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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