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NCT06785506Active, not recruiting

Multiple-biomarker Approach for Individualized Treatment of Heart Failure With Preserved Ejection Fraction

A Dynamic, Multiple-biomarker Approach Aiming for Individualized Treatment of Heart Failure With Preserved Ejection Fraction (ADAPT-HFpEF)

Source: ClinicalTrials.gov · Last updated 7 Oct 2026

Brief summary (registry, in English)

The primary objective is to investigate the association between temporal evolutions of blood biomarkers and clinical adverse events, in order to produce a dynamic, individual, and accurate prediction model for patients with HFpEF. Moreover several secondary objectives will be investigated.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
15 Jul 2024
Start date
25 Nov 2022
Primary completion date
1 Nov 2026
Lead sponsor
Erasmus Medical Center
NCT number
NCT06785506

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 25 Nov 2022 to the primary completion date, 1 Nov 2026
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Scheduled for surgery or intervention for both coronary and non-coronary indication within 6 months of inclusion

Other illness

  • Congenital heart disease
  • Coexistent condition with life expectancy of \<1 year

Lab values

  • History of LVEF ≤40%
  • Impaired renal function, defined as eGFR \< 20 mL/min/1.73 m2 (CKD-EPI) or requiring dialysis at the time of screening
  • Acute or chronic liver disease, defined by serum levels of transaminases or alkaline phosphatase more than three times the upper limit of normal at screening

Other

  • COPD Gold stage IV
  • Pregnancy
  • Unlikely to appear at all scheduled follow-up visits
  • Linguistic barrier

Who the study is looking for

  • Age of 18 years or older
  • Capable of understanding and signing informed consent
  • A diagnosis of HFpEF according to the HFA-PEFF diagnostic algorithm of the ESC or/and a high (90%) probability of HFpEF according to the H2FPEF score, i.e. a score of 6 or higher.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Noordwest Ziekenhuisgroep
Coordinator of this site? Confirm its status
AlkmaarNetherlandsUnknown status
Amsterdam UMC
Coordinator of this site? Confirm its status
AmsterdamNetherlandsUnknown status
OLVG Ziekenhuis
Coordinator of this site? Confirm its status
AmsterdamNetherlandsUnknown status
Erasmus MC
Coordinator of this site? Confirm its status
RotterdamNetherlandsUnknown status
Ikazia Ziekenhuis
Coordinator of this site? Confirm its status
RotterdamNetherlandsUnknown status
Franciscus Gasthuis & Vlietland Ziekenhuis
Coordinator of this site? Confirm its status
RotterdamNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.