Actively Recruiting

Phase 2
Phase 3
Age: 18Years +
All Genders
NCT06423599

Effect of Weight Loss on Physical and Cardiac Performance in People With Obesity and Heart Failure

Led by Jens D Hove, MD,PHD · Updated on 2024-05-24

100

Participants Needed

1

Research Sites

136 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The benefit of weight loss in patients with obesity and heart failure with reduced ejection fraction (HFrEF) is controversial. Semaglutide has shown cardiovascular (CV) risk-reduction and impact on CV risk factors including overweight, dysglycaemia and hypertension in subjects with type 2 diabetes (T2D). The STEP-HFpEF (Semaglutide Treatment Effect in People With Obesity and HFpEF) recently demonstrated, at 1-year, to not only reduce weight considerably, but also significantly improve health-related quality of life, functional status scores and 6-min walk distance in patients with heart failure with preserved ejection fraction (HFpEF). Also, the recently concluded SELECT trial was the first CV outcome trial with semaglutide in patients with overweight or obesity and established CV disease, including heart failure (but no T2D). Semaglutide demonstrated a 20% reduction in MACE, defined as the composite of cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke. These landmark findings have important implications for clinicians -as they mean that weight loss and/or semaglutide as anti-obesity pharmacotherapy could be a treatment strategy for secondary prevention of CV disease in patients with overweight or obesity. It is, however, unknown whether weight loss with either calorie-restricted diet or semaglutide has beneficial effects in obese subjects with heart failure and reduced ejection fraction. Also it is unclear whether semaglutide has cardiovascular benefits irrespective of starting weight and amount of weight loss. Purpose: The study aims to investigate whether weight loss treatment with semaglutide is superior to weight loss with calorie-restricted diet in improving peak oxygen uptake in patients with obesity and heart failure with reduced ejection fraction.

CONDITIONS

Official Title

Effect of Weight Loss on Physical and Cardiac Performance in People With Obesity and Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female, age 18 years or older at the time of signing informed consent
  • Body mass index (BMI) of 30 kg/m2 or higher
  • Diagnosis of heart failure with New York Heart Association (NYHA) class 1 to 3 and reduced ejection fraction (EF 640%) confirmed by echocardiography and/or cardiac magnetic resonance
  • On stable optimal medical heart failure therapy for at least 4 weeks
Not Eligible

You will not qualify if you...

  • Myocardial infarction, stroke, hospitalization for unstable angina pectoris, or transient ischemic attack within 6 months before screening
  • Planned coronary, carotid, or peripheral artery revascularization known at screening
  • Transient heart failure due to reversible causes such as tachycardia or sepsis
  • Type 1 diabetes
  • Treatment with any glucagon-like peptide-1 (GLP-1) agonists within 90 days before screening
  • Type 2 diabetes requiring medications other than metformin and sodium-glucose cotransporter-2 (SGLT2) inhibitors
  • Pregnancy or planned pregnancy
  • History or presence of chronic pancreatitis
  • Acute pancreatitis within 180 days before screening
  • Kidney disease with estimated glomerular filtration rate (eGFR) less than 35 ml/min
  • History or presence of malignant tumors within 5 years before screening (except basal or squamous cell skin cancer and carcinoma in situ)
  • Known or suspected allergy to trial products or related substances

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Amager and Hvidovre Hospital University of Copenhagen

Copenhagen, Denmark, DK-2650

Actively Recruiting

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Research Team

J

Jens D Hove, MD, PhD

CONTACT

M

Mohammed El-Sheikh, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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