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NCT07468344Recruiting

Evaluation of the Effects of Sauna Therapy on Congestion and Loop Diuretic Use in Patients With Heart Failure With Reduced or Moderately Reduced Ejection Fraction

Impact of Sauna Therapy on Congestion and Loop Diuretic Adjustment in Patients With Heart Failure

Source: ClinicalTrials.gov · Last updated 29 Oct 2026

Brief summary (registry, in English)

This study aims to evaluate the effect of sauna therapy on congestion levels during cardiac rehabilitation in patients with heart failure who have an impaired or moderately impaired ejection fraction, compared to standard cardiac rehabilitation care. To investigate this, patients with reduced cardiac function who are hospitalized as part of a cardiac rehabilitation program will be included. These patients will be randomly assigned to two groups: standard cardiac rehabilitation program (control group) and sauna group (intervention group). The study will also assess whether this approach could allow for a reduction in the dose of diuretics, which are commonly used to remove excess fluid, thereby helping to avoid certain side effects. The expected benefits include a reduction in symptoms such as shortness of breath and swelling, improvements in quality of life and physical fitness, and enhanced blood vessel function.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
46 (estimated)
First submitted
12 Feb 2026
Start date
23 Jun 2026
Primary completion date
23 Sept 2027
Lead sponsor
Central Hospital, Nancy, France
NCT number
NCT07468344

What you commit to

  • Study type: Interventional
  • Planned participants: 46
  • From 23 Jun 2026 to the primary completion date, 23 Sept 2027
  • 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

  • Person presenting a contraindication to sauna therapy (for example, intolerance to heat).
  • Person subject to Articles L. 1121-5, L. 1121-7, and L. 1121-8 of the Public Health Code (applicable in France) :- pregnant, giving birth, or breastfeeding woman , minor (non-emancipated), person adult subject to a legal protection measure (guardianship, curatorship, judicial protection) , adult unable to express consent, persons deprived of liberty by judicial or administrative decision, persons receiving psychiatric care under Articles L. 3212-1 and L. 3213-1…

Other illness

  • Active infection, liver disease, or peripheral vascular disease.
  • Acute coronary syndrome or recent stroke (\<90 days).

Lab values

  • Serum sodium \< 130 mmol/L.
  • Serum potassium \> 5.5 mmol/L.

Other

  • Participation in another interventional clinical trial.
  • Person who objects to the processing of their data for quality control purposes

Who the study is looking for

  • Age ≥ 18 years.
  • Heart failure with ejection fraction \<50% confirmed by an echocardiogram within the past year.
  • NYHA class II-III.
  • Loop diuretic dose ≥ 40 mg/day of furosemide (or equivalent) for at least 30 days.
  • NT-proBNP \> 400 pg/ml or BNP \> 100 pg/ml.
  • Estimated glomerular filtration rate (eGFR) ≥ 20 ml/min/1.73 m².
  • Patient scheduled for a hospital-based cardiac rehabilitation program for a minimum of 3 weeks.
  • Person who has undergone a preliminary clinical examination suitable for clinical research.
  • Person affiliated with a social security system or a beneficiary of such a system.
  • Person who has received complete information about the organization of the clinical research and has signed informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
Centre Hospitalier Régional Universitaire de Nancy
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NancyFranceRecruiting

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