Blood marker may reveal kidney trouble early in heart failure patients
NCT ID NCT00561483
First seen Jun 27, 2026 · Last updated Jul 24, 2026 · Updated 2 times
Summary
This study looked at 64 adults hospitalized for acute heart failure to see if a blood marker called cystatin C could detect early kidney problems caused by diuretic treatment. Researchers measured cystatin C levels daily and compared them to standard kidney tests. The goal was to understand how kidney function changes during treatment and whether cystatin C could help predict worsening kidney function in the future.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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64 people
The number who actually took part.
- Started
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Dec 2007
- Finished
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Oct 2016
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients admitted to the hospital with decompensated heart failure
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Hospital admission within 48 hours for ADHF, with an expected stay over 24 hours. * Evidence of fluid overload, including jugular venous distention, pulmonary rales, peripheral edema, and/or ascites receiving diuretic therapy Exclusion Criteria: * Heart failure due to congenital heart disease or critical aortic stenosis (potentially different cardio-renal pathophysiology) * Acute myocardial infarction or unstable acute coronary syndromes * End-stage renal insufficiency on renal replacement therapy (already has underlying advanced renal failure). * Patients with active cancer (cystatin C has been shown to be produced by some tumors) * Known exposure to nephrotoxic agents (such as contrast dye) or planned surgery during hospitalization at the time of enrollment * Hemoglobin \< 9 mg/dL or clinically significant active bleeding. * Unable to comply with protocol or unable to have informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cleveland Clinic
Cleveland, Ohio, 44195, United States
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Other studies related to the condition(s) this trial covers.
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