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Clinical Trial Summary

To investigate the effect of nutritional supplement on bone turnover markers (which are sensitive and respond quickly to nutrition or drug intervention) in Indian healthy premenopausal women after 6 months of intervention.


Clinical Trial Description

This will be a double blind, single-center, randomized-controlled trial testing the effect of fortified beverage on bone turnover markers as compared to placebo control in 25-45 years old premenopausal women. The study will consist of two groups: Group 1 (Test) - Protein rich beverage powder fortified with MMN and Group 2 (control) - Low protein non-fortified iso-caloric beverage powder. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03155269
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date May 25, 2017
Completion date January 16, 2018

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