Clinical Trial on a Natural Compound to Improve Chronic Inflammation After SARS-CoV-2 Infection (NCT07397910) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Clinical Trial on a Natural Compound to Improve Chronic Inflammation After SARS-CoV-2 Infection
Spain40 participantsStarted 2026-02-23
Plain-language summary
A controlled, randomized clinical trial is proposed to demonstrate the effectiveness of the experimental product in controlling hepato-pulmonary inflammation and neurovascular encephalic inflammation, which may constitute the etiopathogenic basis of persistent COVID. In addition, an individualized training program will be implemented for each participant in order to improve chronic symptoms and, consequently, their quality of life.
Who can participate
Age range18 Years – 70 Years
SexALL
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Inclusion Criteria:
* Subjects of both sexes.
* Subjects over 18 and under 70 years of age who have had a SARS-CoV-2 infection diagnosed by PDIA.
* Subjects with a history of SARS-CoV-2 infection who, three months after the onset of COVID-19, continue to experience symptoms lasting at least two months that cannot be explained by another cause. These symptoms may be newly developed after initial recovery from an acute COVID-19 episode or persist from the initial illness.
* No history of sequelae from a severe acute illness.
Exclusion Criteria:
* Subjects with an underlying disease that explains the clinical manifestations.
* Presence of chronic inflammatory diseases.
* Subjects with acute infections.
* Evidence of active thromboembolic disorder, defined as those receiving parenteral anticoagulant or thrombolytic treatment.
* Excessive alcohol consumption.
* Hypersensitivity or intolerance to any of the components of the study products.
* Use of any nutraceutical or dietary supplement.
* Severe or terminal illnesses.
* Subjects with a body mass index (BMI) over 32.
* Pregnant or lactating women.
What they're measuring
1
Immunoinflammatory profile
Timeframe: Blood samples will be taken twice, once at baseline, at the beginning of the trial and once at the end after 120 days of product intake.
Trial details
NCT IDNCT07397910
SponsorUniversidad Católica San Antonio de Murcia