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Primary end points also included hospitalization and oxygen requirements, with severity parameters defined by CDC pneumonia criteria ( Study secondary end points included the comparison of ACE1 and ACE2 receptor levels between the supplement and placebo groups of Cohort 2 (analyzed at baseline and every 7 days for 21 days) and the ACE1/ACE2 ratios in both supplement and placebo groups of each cohort
A subsequent randomized placebo-controlled study from the same center did not show a significant difference in outcomes, including objective curvature improvement (76)
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doi: 10.1111/head.14099 198
