Could a heart pill beat long COVID fatigue? new trial aims to find out.
NCT ID NCT05697640
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether the drug vericiguat, already approved for heart failure, can improve physical function and reduce fatigue in people aged 18-50 with post-COVID syndrome. About 104 participants will receive either vericiguat or a placebo for 10 weeks, then be followed for 30 days. The goal is to see if the drug helps with daily activities like walking and carrying groceries.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 104 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 50 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Male or female adult who is 18-50 years old * Confirmed (PCR or serology), non-hospitalized, mild to moderate acute COVID-19 cases according to WHO criteria with proven chronic ED and either: ME/CFS Canadian Consensus Criteria (CCC) with post exertional malaise (PEM) 2 - 14 hours = PCS or ME/CFS CCC criteria with PEM \> 14 hours = PCS/CFS * Ongoing symptoms of PCS or PCS/CFS for ≥ 6 months * Bell Score: 30-60 * Evidence for endothelial dysfunction (ED) \[as indicated by reactive hyperemia index (RHI) \< 1.8 and/or ET-1 level \> 90 percentile of healthy age- and gender matched controls or muscle fatigue (below cut-off values of area under the curve reference values for age-matched healthy controls and/or pathological optical coherence tomography angiography (OCTA))\] * For female subjects: Confirmed post-menopausal state (defined as amenorrhea for at least 12 months) or for women of childbearing potential: Negative highly sensitive urine or serum pregnancy test before inclusion/randomisation and practicing a highly effective birth control method (failure rate of less than 1 %): * combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral/intravaginal/transdermal), or * progestogen-only hormonal contraception associated with inhibition of ovulation (oral/injectable/implantable), or * intrauterine device, or * intrauterine hormone-releasing system, or * bilateral tubal occlusion, or * vasectomised partner, or * heterosexual abstinence. Exclusion Criteria: * COVID-19 vaccination within the last 4 weeks before inclusion * Pre-COVID history of chronic fatigue syndrome or other fatigue syndromes that are due to associated diseases (e.g., cancer, autoimmune diseases \[patients with a preexisting Hashimoto thyroiditis and/or fibromyalgia without fatigue syndromes can be included\]) * Concomitant use of Vericiguat due to other diseases * Contraindications against IMP * Concurrent or anticipated concomitant use of PDE-5 inhibitors such as vardenafil, tadalafil, and sildenafil, nitrates, or sGC-stimulators * Use of other sGC stimulators, e.g., riociguat * Hypersensitivity to the active substance or any of the other ingredients * Systolic blood pressure: \< 100 mmHg at screening * Known SARS-CoV-2 infection-related organ damage/comorbidity * Severe renal or hepatic insufficiency * Pregnancy or breastfeeding
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Charité - Universitätsmedizin Berlin
Berlin, State of Berlin, 10117, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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