Geneva, Aug. 5 -- International Clinical Trials Registry received information related to the study (ISRCTN14209798) titled 'Evaluating the effects of daily microgreen powder supplementation over 60 days on fatigue and nutrition-related symptoms among women of reproductive age in Yangon, Myanmar' on July 18.
Study Type: Interventional
Study Design:
Waitlist-controlled single-centre interventional trial using block randomisation with blinded outcome assessors (Prevention)
Primary Sponsor: Hebrew University of Jerusalem
Condition:
Dietary micronutrient deficiency
Nutritional, Metabolic, Endocrine
Intervention:
Group A (intervention): Receives 10 g of microgreen powder daily, made from an equal blend of sunflower, mung bean and musta...