Clinical Trial on a Natural Compound to Improve Chronic Inflammation After SARS-CoV-2 Infection
NCT07397910 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2026-02-09
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.
Conditions
Interventions
- DIETARY_SUPPLEMENT
-
Experimental Product
Supplement consisting of orange extract, apigenin, luteolin, yerba mate extract, grapefruit extract, and olive leaf extract.
- DIETARY_SUPPLEMENT
-
Control placebo
Product with identical characteristics to the experimental product.
- OTHER
-
Physical exercise
During the study, subjects will have to develop a training program. A multicomponent program will be carried out during the 4 months of product consumption. The sessions will last 60 minutes and will be held 2-3 times per week.
- OTHER
-
No Physical Exercise
During the study, subjects will only consume the product assigned to them in the randomization.
Sponsors & Collaborators
-
Universidad Católica San Antonio de Murcia
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-02-23
- Primary Completion
- 2026-07-06
- Completion
- 2026-08-03
Countries
- Spain
Study Locations
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