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NCT Number: NCT07243119

PRIMA-HF: Predicting Myocardial Recovery in Heart Failure Using Cardiac Imaging HAI-HF: High Dosing vs. Standard Dosing Adenosine During Myocardial Perfusion in Heart Failure

Background:

Heart failure with reduced ejection fraction (HFrEF) is a heterogeneous condition with variable potential for left ventricular ejection fraction (LVEF) recovery. While LVEF improvement and reverse remodeling predict better outcomes, the determinants that predict left ventricular recovery remain poorly understood. An expert panel of the Journal of American College of Cardiology highlighted the need for improved HFrEF phenotyping to clarify recovery patterns and support personalized management and risk stratification.

Methods:

PRIMA-HF is a prospective prediction study designed to determine whether baseline cardiac multimodality imaging can predict LVEF recovery in patients with de novo HFrEF (n=180). The imaging protocol includes cardiac magnetic resonance (CMR), coronary computed tomography and [¹⁵O]H₂O positron emission tomography ([¹⁵O]H₂O-PET) and echocardiography. Patients will also undergo a six-minute walk test, blood volume measurement, and blood sampling. The primary outcome is the change in LVEF from baseline to approx. after 3-12 months (or after full optitration in GDMT), assessed by CMR.

In 60 patients from the PRIMA-HF cohort, the randomized, double-blind study High Dose Adenosine During Perfusion Imaging in Heart Failure (HAI-HF) will be conducted. HAI-HF evaluates whether high-dose adenosine (210 µg/kg/min) versus standard-dose (140 µg/kg/min) during [¹⁵O]H₂O-PET changes the stress myocardial blood flow, which is the primary endpoint.

Aim:

The PRIMA-HF study comprehensively characterizes patients with newly diagnosed HFrEF through multimodality imaging and systematically assesses change in LVEF using CMR. The study's deep phenotyping approach integrates clinical, imaging, biomarker, and functional data to capture disease heterogeneity, rather than relying on traditional measures such as LVEF or symptom class. This enables the identification of distinct patient subgroups with shared pathophysiological mechanisms.

The HAI-HF trial examines whether higher adenosine doses improve [¹⁵O]H₂O-PET perfusion imaging in HFrEF.

Together, the studies will advance understanding of myocardial recovery, improve perfusion assessment, and support development of a predictive model for HFrEF prognosis.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University Clinic of Cardiovascular Reseach

Herning, 7400, Denmark

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • Capable and has provided written informed consent
  • LVEF ≤ 40% by echocardiography in connection with hospitalization for heart failure or in connection with outpatient evaluation for heart failure

Exclusion criteria

  • Previous diagnosis of heart failure
  • Unable to understand the patient information
  • Pregnancy, as the study involves ionizing radiation.
  • Current severe valvular disease (as defined by the Danish national treatment guidelines on cardio.dk)
  • Atrial fibrillation with a heart rate > 130 beats per minute during the inclusion echocardiography
  • Cardiac surgery within 6 months prior to inclusion
  • Acute exacerbation of existing chronic obstructive pulmonary disease
  • Severe asthma or chronic obstructive pulmonary disease with FEV1 < 1L
  • any contraindication for adenosine stress testing
  • Severe renal failure < 15 mL/min/1.73m² or dialysis
  • Advanced liver disease (Child-Pugh class C)
  • Endocarditis at inclusion/baseline
  • Isolated right-sided heart failure
  • Malignant disease treated with chemotherapy or radiotherapy, or expected life expectancy under 1 year

Treatment and study plan

HAI-HF: Adenosine Stress [¹⁵O]H₂O PET Imaging

Diagnostic Test

HAI-HF: Patients will be randomized in a 1:1 ratio to one of two dosing sequences: high-dose followed by low-dose adenosine, or low-dose followed by high-dose adenosine.

Two different doses of adenosine

Drug

Testing if high dose adenosine (210 ug/kg/min) during perfusion imaging results in a higher myocardial blood flow compared to standard dose (140 ug/kg/min) in patients with HFrEF

Primary outcomes

  1. PRIMA-HF: Left ventricular ejection fraction (LVEF)

    Time frame: PRIMA-HF: Baseline through study completion, an average of 3 months

    Change in LVEF (continuous variable, absolute change in LVEF in percent points)

  2. HAI-HF: Stress Myocardial Blood Flow (MBF)

    Time frame: Baseline and periprocedural

    Change in stress MBF (continuous variable, ml/min/g)

Secondary outcomes

  1. PRIMA-HF: Kansas City Cardiomyopathy Questionaire (KCCQ-12)

    Time frame: Baseline through study completion, an average of 3 months

    Change in Kansas City Cardiomyopathy Questionnaire (KCCQ-12) (points, continuous data)

  2. PRIMA-HF: 6 minutes-walk-test

    Time frame: Baseline through study completion, an average of 3 months

    Change in 6MWT distance (meters, continuous data)

Other outcomes

  1. PRIMA-HF: Blood volume

    Time frame: Baseline through study completion, an average of 3 months

    Change in blodvolume (L, continuous data)

  2. PRIMA-HF: NT-Pro-BNP

    Time frame: Baseline through study completion, an average of 3 months

    Change in NT-Pro-BNP (pg/mL or pmol/L, continuous data)

Sponsors and collaborators

Lead sponsor

Gødstrup Hospital

Other

Registry information

Official study title

PRIMA-HF PRedicting Recovery of Left Ventricular Function With Multimodality Cardiac IMAging in Patients With de Novo Heart Failure HAI-HF: High-Dose Adenosine During Perfusion Imaging in Heart Failure: Rationale and Design of the HAI-HF Trial

Acronym: PRIMA-HF

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Nov 21, 2025
Registry last updated
Dec 26, 2025

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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