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Clinical Trial Summary

The aim of this randomised clinical trial study is to evaluate whether supplementation with vitamin D could reduce the risk of uterine fibroids in reproductive stage women.


Clinical Trial Description

A total of 1160 hypovitaminosis D patients (12 ng/ml ≤ serum 25-hydroxyvitamin D3 < 20 ng/ml) without uterine fibroids will be randomly assigned in a ratio of 1:1 to two groups: intervention group and control group. The intervention group will receive 1600 IU/d of vitamin D3; the control group will receive regular follow-up. Patients will be followed up at the same time points for 24 months. The outcome measure is the incidence of uterine fibroids in different groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03586947
Study type Interventional
Source Second Affiliated Hospital of Wenzhou Medical University
Contact Xueqiong Zhu, PHD
Phone 13906640759
Email zjwzzxq@163.com
Status Not yet recruiting
Phase N/A
Start date September 15, 2018
Completion date July 1, 2021

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