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OpenTrials
Completed

NCT Number: NCT00860340

Hemodynamic Effects of Spironolactone in Patients With Heart Failure

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.

Completed

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Medical University of Ohio

Toledo, Ohio, 43614, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • CHF
  • 21 - 80 years
  • Serum creatinine < 2 mg/dL
  • Serum potassium 2.7 - 4.5 mg/dL measured within past 4 weeks

Exclusion criteria

  • Less than 21 years
  • Pregnancy

Treatment and study plan

Spironolactone

Drug

100 mg tablet of Spironolactone (Aldactone) by mouth with half a glass of water.

Primary outcomes

  1. Echocardiogram

    Time frame: 3 measurements 15 minutes apart before drug and 15 minutes for 2 hours after drug

  2. Measure of Kidney function and potassium levels

    Time frame: This will be taken before drug, two hours after and the following day

Sponsors and collaborators

Lead sponsor

University of Toledo Health Science Campus

Other

Registry information

Important dates

Study start
2003
Primary completion
2006
Study completion
2006
First posted
Mar 12, 2009
Registry last updated
Dec 10, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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