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NCT07539766Recruiting

OBESE-HFpEF: Towards Preventing Obesity Related HFpEF

OBESE-HFpEF: Prevalence and Mediators of Heart Failure (Preserved Ejection Fraction) in the Dutch Obesity Clinic South - Towards Preventing Obesity Related HFpEF''

Source: ClinicalTrials.gov · Last updated 20 Apr 2026

Brief summary (registry, in English)

Obesity, severe overweight, is a growing problem worldwide and increases the risk of heart failure, especially a type called heart failure with preserved ejection fraction (HFpEF). In HFpEF, the heart becomes stiffer. This makes it harder for the heart to fill with blood, which can lead to shortness of breath during physical activity. In the Netherlands, 15% of the population has obesity. In South Limburg, this is even higher at 19%. Among people with HFpEF, obesity is much more common: about 50% of these patients have obesity. Life expectancy in people with HFpEF is poor, and current treatment mainly focuses on reducing symptoms. Early recognition and treatment of risk factors, such as obesity, are therefore very important. This study includes about 250 people with obesity. Using a heart ultrasound and tests of blood and fat tissue, we will look for early signs of HFpEF and study the effects of weight loss. The measurements will be repeated after 1 and 2 years. The goal of this study is to better understand how obesity contributes to HFpEF and how weight loss affects the heart. This research may help improve future treatments for patients with HFpEF.

Status (registry)
Recruiting
Study type
Observational
Enrollment
250 (estimated)
First submitted
30 Jan 2026
Start date
1 Jan 2025
Primary completion date
1 May 2028
Lead sponsor
Zuyderland Medisch Centrum
NCT number
NCT07539766

What you commit to

  • Study type: Observational
  • Planned participants: 250
  • From 1 Jan 2025 to the primary completion date, 1 May 2028
  • 1 site 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

  • Inability of undergoing metabolic bariatric surgery safely.
  • A medical history of previous metabolic bariatric surgery.

Lab values

  • A medical history of a reduced LVEF at any time, history of severe cardiac valve defects or severe congenital cardiac defects.

Other

  • Inability to provide informed consent.
  • A BMI \>60 kg/m2
  • Inability to undergo the study measurement/tests.
  • Not proficient in the Dutch language

Who the study is looking for

  • Age ≥ 35 years
  • Eligible for surgical treatment for obesity, according to the Dutch guideline, i.e. a BMI ≥ 40 kg/m2 or a BMI ≥ 35 kg/m2 with one or more comorbidities associated with obesity. (23)

Age in the registry: 35 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Zuyderland Medisch Centrum - Heerlen
Coordinator of this site? Confirm its status
HeerlenNetherlandsRecruiting

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