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Recruiting NCT05931614

NCT05931614 Liberal or Restricted Fluid Intake in Patients With Heart Failure

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Clinical Trial Summary
NCT ID NCT05931614
Status Recruiting
Phase
Sponsor Region Stockholm
Condition Heart Failure
Study Type INTERVENTIONAL
Enrollment 326 participants
Start Date 2024-02-14
Primary Completion 2028-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Free fluid intake

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 326 participants in total. It began in 2024-02-14 with a primary completion date of 2028-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Heart failure is the most common cause of admission to hospital and is associated with high morbidity and mortality. Treatment options consist of medical- and device treatment and self-care strategies, where fluid restriction has been one of the components in the self-care management of patients with chronic heart failure. The medical treatment has progressed and improved over the years and considerably over the last few years, which has decreased symptoms and improved physical function of these patients. Despite our great success in the medical treatment of heart failure, we still face challenges in hospital readmissions and treatment strategies. It contributes to the increased need of evidence on, if and how, fluid intake and fluid restriction should be used as a self-care method. Fluid restriction as a self-care treatment is still commonly recommended in heart failure management although the scientific clinical evidence is lacking. Fluid restriction is associated with a higher degree of thirst and lower rated quality of life, and there is no consensus on how fluid restriction should be used, no plan for individualized treatment and no agreement on how fluid restriction should be a part of the patient self-care treatment. There is therefore a need for knowledge on how heart failure patients are affected by fluid restriction regarding clincal signs and symptoms of heart failure, quality of life, physical function, readmission to hospital or heart failure events. The primary aim of the study is to investigate whether a free fluid intake is safe compared to a restricted fluid intake, regarding clinical signs of heart failure measured as the presence of B-lines and/or an increase in NT-proBNP. The secondary aim is to clarify whether an unlimited fluid intake can improve quality of life and reduce thirst without affecting heart failure symptoms, physical activity, hospital readmissions and/or heart failure events.

Eligibility Criteria

Inclusion Criteria: * Diagnosed with left ventricual heart failure (HFrEF, HFmEF) * Physical, cognitive and linguistic ability to carry out all aspects of the study Exclusion Criteria: * Reversible cause of HF (thyroid disorders, severe anemia, etc.) * Hyponatremia at baseline (sodium \<130 mmol/L) * eGFR at baseline \<30mL/min/1.73m2 * Scheduled cardiac surgery, coronary intervention (percutaneous coronary intervention or coronary artery bypass graft surgery) within 3 months * Myocardial infarction within 3 months * Comorbidity for which fluid restriction or unlimited fluid intake is advised * Life expectancy \<6 months

Contact & Investigator

Central Contact

Carolin Nymark, PhD

✉ carolin.nymark@ki.se

📞 +46725955887

Principal Investigator

Carolin Nymark, PhD

PRINCIPAL INVESTIGATOR

Karolinska Universitetssjukhuset, Heart and Vascular Center

Frequently Asked Questions

Who can join the NCT05931614 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Heart Failure. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05931614 currently recruiting?

Yes, NCT05931614 is actively recruiting participants. Contact the research team at carolin.nymark@ki.se for enrollment information.

Where is the NCT05931614 trial being conducted?

This trial is being conducted at Stockholm, Sweden.

Who is sponsoring the NCT05931614 clinical trial?

NCT05931614 is sponsored by Region Stockholm. The principal investigator is Carolin Nymark, PhD at Karolinska Universitetssjukhuset, Heart and Vascular Center. The trial plans to enroll 326 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology