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Study to assess the efficacy of ginsana in improving half-time hemoglobin re-oxygenation in healthy, recreational sportspeople and to assess the safety of the product
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| GINSANA | Experimental |
| |
| Placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| GINSANA | Drug |
| ||
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in half-time hemoglobin re-oxygenation by Near InfraRed Spectroscopy (NIRS) methodology | Baseline, day 84 post first drug dispense |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in half-time hemoglobin re-oxygenation by NIRS methodology | Baseline, day 21, 42 and 63 post first drug dispense | |
| Maximum endurance time | up to day 84 post first drug dispense |
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Inclusion Criteria:
Exclusion Criteria:
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|
| Change from baseline in respiratory threshold | Baseline, up to day 84 post first drug dispense |
| Change from baseline in thiobarbituric acid (TBARS) | Baseline, up to day 84 post first drug dispense |
| Change from baseline in glutathion superdismutase / glutathion superdismutase oxidised (GSA/GSSG) | Baseline, up to day 84 post first drug dispense |