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Study identifier: NCT07234422 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingSELEQT-HF

The SELEQT-HF (SELEnium and CoQ10 NuTrition for Heart Failure) Study Will Evaluate the Effect of Adding Selenium/and coQ10 on Top of Standard HF Therapy in Patients With HF and Will do so Using a Pragmatic, Registry Based Randomized Controlled Trial in the Netherlands.

Condition: Heart Failure  ·  Sponsor: Netherlands Heart Institute

PhasePhase 3
Planned participants1100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where7 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The goal of this clinical trial is to learn whether taking selenium and coenzyme Q10 (CoQ10) can reduce HF related events and deaths related to cardiovascular disease. Researchers will compare selenium-CoQ10 supplements with a placebo to see if the supplements improve heart health and patient outcomes. Participants will: Receive either selenium-CoQ10 or placebo in addition to their usual heart failure treatment Attend standard clinical visits according to routine clinical care. The study will include 1,100 adults with chronic heart failure. Selenium and CoQ10 are natural nutrients with no known health risks. If effective, this supplement could provide a safe new way to improve outcomes for people with heart failure.

This description comes directly from the study's public registry record.

Talk to the study team

SELEQT-HF Study Team  ·  +31 (0)503616161  ·  seleqt-hf@umcg.nl

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Age \>18 years * Outpatients with chronic HF, NYHA II - ambulatory IV * Serum NT-proBNP concentrations \>600 pg/mL (71 pmol/L) if in sinus rhythm; \>1000pg/mL (118 pmol/L) if in Atrial fibrillation\* Exclusion Criteria: * History of myocardial infarction, myocarditis, percutaneous intervention, cardiac surgery or stroke \<30 days * The presence of a mechanical assist device * Scheduled for mechanical assist device or heart transplant * Other non-cardiac conditions with limited life expectancy (\<1 year) * Amyloid, hypertrophic obstructive or constrictive cardiomyopathy * End stage kidney disease for which chronic intermittent peritoneal or haemodialysis * Unable to sign informed consent * (Unwilling to stop) use of over the counter supplements coQ10/selenium * Peanut and/or soy allergy

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (7)

Noordwest ZiekenhuisgroepAlkmaar, NetherlandsNot Yet Recruiting
AUMCAmsterdam, NetherlandsNot Yet Recruiting
Amphia ZiekenhuisBreda, NetherlandsRecruiting
Catharina ziekenhuis EindhovenEindhoven, NetherlandsNot Yet Recruiting
TREANTEmmen, NetherlandsNot Yet Recruiting
University Medical Center GroningenGroningen, NetherlandsRecruiting
St Antonius ziekenhuisNieuwegein, NetherlandsNot Yet Recruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

BredaGroningenAlkmaarAmsterdam

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