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临床试验/NCT07243119
NCT07243119Enrolling By Invitation4 期

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

Gødstrup Hospital1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2025年12月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
Enrolling By Invitation
发起方
入组人数
180
试验地点
1
主要终点
PRIMA-HF: Left ventricular ejection fraction (LVEF)

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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

研究组 & 干预措施

High-dose then Low-dose Adenosine

Experimental

干预措施: Two different doses of adenosine (Drug)

Low-dose then High-dose Adenosine

Experimental

干预措施: Two different doses of adenosine (Drug)

结局指标

主要结局

PRIMA-HF: Left ventricular ejection fraction (LVEF)

时间窗: PRIMA-HF: Baseline through study completion, an average of 3 months

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

HAI-HF: Stress Myocardial Blood Flow (MBF)

时间窗: Baseline and periprocedural

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

次要结局

  • PRIMA-HF: Kansas City Cardiomyopathy Questionaire (KCCQ-12)(Baseline through study completion, an average of 3 months)
  • PRIMA-HF: 6 minutes-walk-test(Baseline through study completion, an average of 3 months)

研究者

发起方
Gødstrup Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sarah Lindhøj Kvorning

Principal Investigator, MD, PhD student

Gødstrup Hospital

研究点 (1)

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