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Sauna sessions may ease heart failure symptoms and reduce water pills

NCT ID NCT07468344

Symptom relief Sponsor: BAUDRY Guillaume Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether adding sauna therapy to standard cardiac rehabilitation can help people with heart failure feel less congested and possibly lower their dose of water pills (diuretics). About 46 adults with heart failure and reduced pumping ability will be randomly assigned to either usual rehab or rehab plus sauna sessions. The goal is to ease symptoms like shortness of breath and swelling, and improve quality of life.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 46 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Jul 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * 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. * Systolic blood pressure ≥ 100 mmHg. * 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. Exclusion Criteria: * Person presenting a contraindication to sauna therapy (for example, intolerance to heat). * Serum sodium \< 130 mmol/L. * Serum potassium \> 5.5 mmol/L. * Active infection, liver disease, or peripheral vascular disease. * Acute coronary syndrome or recent stroke (\<90 days). * Participation in another interventional clinical trial. * 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…

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Conditions

The condition(s) this trial relates to.

heart failure systolic heart failure

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Heart failure

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Centre Hospitalier Régional Universitaire de Nancy

    Nancy, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.