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Clinical Trial Summary

Postpartum depression and poor quality of life during postpartum were an vital issue in recent years. Infant's health condition was thought to be a possible reasons related mother's postpartum quality of life, and functional gastrointestinal disorders such as infantile colic and regurgitation were common problem during infant period. Previous study revealed that probiotics may improve the infant's discomfort caused by functional gastrointestinal disorders. Thus, this study aimed to investigate whether probiotics use in neonate and infant improve their mother's life quality?


Clinical Trial Description

This is single blinded intervention study. The investigators will invite mother to participate in the project after giving birth. At week 0, mother who meet the eligibility criteria will be randomized in a single-blind study in a 1:1 ratio to probiotics with Vit. D3 (five drops per day) or Vit. D3 (placebo) (single drop per day) for 90 days. The follow-up will be at the 1, 3 and 6 months all the subjects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04741971
Study type Interventional
Source Buddhist Tzu Chi General Hospital
Contact Yu-Chao Hsiao
Phone 886-3-8561825
Email u9602041@cmu.edu.tw
Status Not yet recruiting
Phase N/A
Start date February 18, 2021
Completion date December 31, 2024

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