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Karolinska-Rennes (KaRen) Prospective Study of Exercise Stress Echocardiography in Heart Failure With Preserved Ejection Fraction

Ancillary Study of the Registry Karolinska-Rennes (KaRen) : Prospective Study of Dyssynchrony in Heart Failure With Preserved Ejection Fraction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00774709
Acronym
KaRen
Enrollment
90
Registered
2008-10-17
Start date
2008-10-31
Completion date
2012-11-30
Last updated
2013-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

Heart failure, Preserved ejection fraction, Diastolic dysfunction, Dyssynchrony, Echocardiography, Patients with acute heart failure clinically, diagnosed, BNP level > 100 ng / l or NT-proBNP > 300 ng /l, Preserved left ventricular ejection fraction(LVEF, ≥ 45%)

Brief summary

Background: Heart failure with preserved ejection fraction (HFPEF) is common but not well understood. Electrical dyssynchrony in systolic heart failure is harmful. Little is known about the prevalence and the prognostic impact of dyssynchrony in HFPEF. Methods: We have designed a prospective, multicentre, international, observational study to characterize HFPEF and to determine whether electrical or mechanical dyssynchrony affects prognosis. Patients presenting with acute heart failure will be screened. Inclusion criteria will be: acute presentation with Framingham criteria for heart failure, left ventricular EF ≥45%, BNP \>100 ng/L or NT-proBNP \>300 ng/L. Patients will return in stable condition 4-8 weeks after the index presentation and undergo questionnaires, serology, ECG and Dopplerechocardiography. Thereafter, patients will be followed for mortality and heart failure hospitalization every 6 months for at least 18 months. Sub-studies will focus on echocardiographic changes from the acute presentation to the stable condition and on exercise echocardiography. Conclusion: KaRen aims to characterize electrical and mechanical dyssynchrony and to assess its prognostic impact in the HFPEF. The ancillary study of the exercise stress echocardiography sought to improve our understanding of HFPEF and generate answers to the question whether dyssynchrony could be a target for therapy in HFPEF.

Interventions

None listed

Sponsors

Fédération Française de Cardiologie
CollaboratorOTHER
French Cardiology Society
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Acute presentation to the hospital with clinical signs and symptoms of HF, according to the Framingham criteria \[19\]. 2. LVEF ≥ 45% by echocardiography within the first 72 hours. The measurement will be carried out according to guidelines 3. BNP \>100 ng/L or NT-proBNP \>300 ng/L.

Exclusion criteria

1. Evidence of primary hypertrophic or restrictive cardiomyopathy or systemic illness known to be associated with infiltrative heart disease 2. Known cause of right heart failure not related to left ventricular dysfunction 3. Pericardial constriction 4. Clinically significant pulmonary disease, as evidenced by requirement of current home oxygen 5. End-stage renal disease currently requiring dialysis 6. Bi-ventricular pacemaker (CRT). (Patients who have a conventional pacemaker may be included) 7. Anticipated or indication for cardiac surgery. (Patients who have indication for surgery but may not undergo surgery because of some contraindication, for example age, may NOT be included). 8. Anticipated percutaneous intervention on aortic stenosis. (Patients who undergo other percutaneous intervention, for example PCI, may be included).

Design outcomes

Primary

MeasureTime frame
Echocardiographic parameter4 to 8 weeks

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026