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Acute Decompensated Heart FailureNCT00762008

Circulating Markers That Underlie the Transition From Compensated Hypertrophy to Heart Failure

An observational study of Acute Decompensated Heart Failure and Heart Failure, run by UConn Health at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of this research is to determine if two proteins in the blood are increased during acute heart failure. These two proteins are produced when the heart becomes dysfunctional and unable to contract normally. Read more about this study

Who is it for?
Ages 18 years and older
How many people
500 participants
Where
1 siteUnited States
Study dates
Dec 2005to Dec 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Recruitment will take place in the University of Connecticut Health Center, both hospital inpatients and Cardiopulmonary clinic out-patients. 1. The target population will be heart failure patients of any etiology. We anticipate that 20% of all recruited subjects will be African American and 5% to be Hispanic. This represents the distribution of populations recruited in the past for heart failure studies. 2. Healthy individuals with no prior history of heart attack or heart failure will be recruited to use as controls.

Who may be able to join

  • Individuals aged >18yrs
  • stable or decompensated heart failure, irrespective of LVEF
  • decompensated heart failure clinical symptoms such as dyspnea, rales, edema, elevated jugular venous pressure, or ascites
  • Imaging evidence of heart failure (cardiomegaly, poor contractile function or echocardiographic Doppler evidence of diastolic dysfunction or elevated right- or left-sided filling pressures)
  • Healthy individuals with no prior history of heart attack or heart failure will be recruited to use as controls.

Who cannot join

  • Subjects who are unable to give informed consent
  • Subjects who had undergone cardiac or non-cardiac surgery in the 3 months before enrollment
  • Pregnant subjects are not excluded

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Kristen Siedlarz, MA contact

860-679-7549

siedlarz@uchc.edu

United States1 site, 1 recruiting
  • University of Connecticut Health Center

    Farmington, Connecticut, 06030

    Recruiting

Other trials in United States

About this study

The purpose of this research is to determine if two proteins in the blood are increased during acute heart failure. These two proteins are produced when the heart becomes dysfunctional and unable to contract normally. They may then be released into the blood and be detected by standard method in the research laboratory. Thus, the purpose of this study is to determine the relation between the change of these two proteins in the blood and the occurrence of acute heart failure. At this time, detection of an increase in these proteins in the blood is not known to be associated with any disease or heart failure.

Read the detailed description

Heart failure (HF) is a complex clinical syndrome and major public health problem claiming the lives of >500,000 per year. It is the leading Diagnosis Related Group (DRG) for hospital discharges in the US. There are approximately 1-3 million admissions annually for acute decompensated heart failure. The mortality rate in Classes III and IV heart failure is 14-18% each year (1). At present, nearly 5 million patients have HF in the U.S. (2). Early detection and prevention remain key measures in treating subjects with this form of heart disease. Discovering and defining circulating markers that underlie the transition between compensated hypertrophy and acute heart failure represent an area of important need in the detection and prevention effort. The existing marker BNP is useful in helping differentiate those with heart failure from those who have other conditions. However, the large variation of abnormal BNP levels in those who carry a diagnosis of heart failure makes BNP level unreliable as a predictor for the transition between compensated and decompensated heart failure.

Apoptosis contributes to, and perhaps, is the cause of myocyte death that underlies the progression of heart dysfunction and the transition between stable compensated heart failure and acute deterioration (3). Apoptosis is a regulated biological process resulting in cell death (4-9). Caspases, a family of cysteine acid proteases regulate the process, and in fact, lead to apoptosis. Apoptotic trigger or signal results in the activation of proximal or initiator caspases (such caspase-8, -9, 10). These initiator caspases then cleave and in turn activate downstream effector caspases such as caspases-3, -6 and -7. These effector caspases then cleave various proteins such as those present in cytoskeletons and nucleus like lamin A, alpha-fodrin and poly (ADP-ribose) polymerase, leading to apoptosis. Caspase-3 is the key executioner in this apoptotic pathway, responsible totally or critically in the proteolytic cleavage of cellular and nuclear proteins. Activation of caspase-3 requires proteolytic processing of its inactive zymogen into active p17 and p12 fragments. The cleaved caspase-3 can be detected by antibodies specific for this cleaved enzyme (p17 fragment) in cell lysates by immunoblotting or by an ELISA assay utilizing spectrophotometric determination with a microplate reader at OD450 nm.

The primary goals of this pilot study are to determine whether 1) activated caspase-3 can be detected in human circulation and if so are there diurnal rhythm variations and serial changes in the levels over time, 2) whether its level is increased during acute decompensated heart failure, and 3) whether transition between acute and stable heart failure is correlated with a decrease in its level.

Another potential marker for acute deterioration is dystrophin. Dystrophin was originally identified as the X-linked gene whose mutations in its N-terminus cause cardiomyopathy. Dystrophin provides important structural support for the cardiac myocyte and its sarcolemmal membrane (10-11). It links actin at its N-terminus with the dystrophin-associated protein complex and sarcolemma at the C-terminus and the extracellular matrix of muscle. Mutations cause loss of support and sarcolemmal instability and myopathy. Myocardial dystrophin translocation and cleavage are associated with the progression of heart failure and contractile dysfunction. These changes are reversed following reduction of mechanical stress from ventricular assistance device (12). In the present pilot study, we will test the hypothesis that dystrophin can be released and detected in human circulation during acute deterioration of heart failure. We will further test whether 1) its level is increased during acute decompensated heart failure, and 2) whether transition between acute and stable heart failure is correlated with a decrease in its level, and 3) whether there are serial changes of these levels over time.

BNP is a known marker for stressed myocardium and has been used to detect myocardial stretching and stress in heart disease. IL-6 and TNF alpha are both inflammatory markers and have been shown to be elevated in inflammatory state such as heart failure. CRP is another inflammatory marker. Knowing their levels is helpful in correlating the serum caspase-3 p17 level with those known serum factors in CHF.

By checking levels of these markers every 3 months (+/- one month) in stable HF patients for two years, our goal is to see if those with a "spike" in level predict adverse outcome in CHF. Ultimately, if such is the case, we can identify patients with a "spike" or cumulative higher caspase-3 fragment as at high risk for morbidity/mortality. Identification of such patients may cause us to treat them more proactively to attempt to alter outcome.

We will also obtain blood samples from control subjects to measure baseline levels and determine if there are diurnal rhythm variations.

Keywords
biomarkers
Medical subject headings
Heart Failure

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00762008
Study groupRoleWhat they receive
Heart FailureNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hospitalization for acute heart failure, myocardial infarction, stroke or death.

    Measured: 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Sep 2008 (estimated)
  2. Study startDec 2005
  3. Primary completionDec 2027 (estimated)
  4. Study completionDec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00762008
Sponsor's protocol ID
06-151-2
Other IDs
08145
Status last verified
Aug 2026
First submitted
26 Sep 2008
Last updated
17 Aug 2026
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Acute Decompensated Heart Failure and Heart Failure, run by UConn Health at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Kristen Siedlarz, MA (860-679-7549, siedlarz@uchc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hospitalization for acute heart failure, myocardial infarction, stroke or death. (time frame: 3 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Aug 2026.

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