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| Name | Class |
|---|---|
| Wroclaw University of Environmental and Life Sciences | OTHER |
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Growing body of evidence indicates favorable effects of Cornus mas (Cornelian cherry) supplements on cardiometabolic risk, including the improvement of HDL and glycemic indices, in line with vascular benefits. Experimental data feature bioactives from Cornelian cherry as potential modulators of vascular function and blood pressure, plausibly via endothelial nitric oxide-related pathways, with possible downstream effects on autonomic reflex control; nevertheless, such links in humans remain poorly explored to date, especially in terms of endurance training and hypoxia tolerance.
In this cross-over, placebo-controlled study, a group of healthy amateur long-distance runners underwent two stages of a four-week dietary intervention (separated by four weeks of washout period), receiving Cornelian cherry lyophilisate or placebo. Each supplementation stage was accompanied by the comprehensive evaluation of the cardio-respiratory parameters and endothelial function.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cornus mas lyophilisate | Experimental |
| |
| placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cornus mas lyophilisate | Dietary Supplement | Participants receiving a Cornus mas (Cornelian cherry) lyophilisate for 4 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Systemic vascular resistance | Resting systemic vascular resistance, evaluated non-invasively with a finger cuff-based device. | From the beginning to the end of a supplementation period at 4 weeks. |
| Office blood pressure values (mean, systolic, diastolic) | Resting arterial blood pressure values (mean, systolic, diastolic), measured continuously with a non-invasive, finger cuff-based device. | From the beginning to the end of a supplementation period at 4 weeks. |
| Measure | Description | Time Frame |
|---|---|---|
| Peripheral chemoreflex sensitivity | Peripheral chemoreflex sensitivity, measured with the transient hypoxia test. | From the beginning to the end of a supplementation period at 4 weeks. |
| eNOS expression |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Wroclaw Medical University | Wroclaw | Lower Silesian Voivodeship | 50-376 | Poland |
This is a small trial which includes solely healthy volunteers. Therefore, data will not be shared at this instance.
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| Placebo | Dietary Supplement | Participants receiving a starch- and sugar-based placebo for 4 weeks. |
|
Endothelial nitric oxide synthase expression, evaluated in the peripheral blood samples.
| From the beginning to the end of a supplementation period at 4 weeks. |