Clinical Trials Directory

Trials / Completed

CompletedNCT03310307

Vitamin D3 Treatment and Homocysteine Concentrations Among Overweight Reproductive Women

Vitamin D3 Treatment Decreases Serum Total Homocysteine Concentrations of Overweight Reproductive Women: Randomized Placebo Controlled Clinical Trail

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Al-Balqa Applied University · Academic / Other
Sex
Female
Age
18 Years – 49 Years
Healthy volunteers
Accepted

Summary

100 overweight reproductive vitamin D deficient women were divided into two groups; vitamin D (n = 50) and placebo (n = 50). Vitamin D group received treatment dose of 50,000 IU of vitamin D3 per week for 2 consecutive months and placebo group received placebo tablets similar in size, shape and color to vitamin D3 for 2 months also. Total homocysteine concentrations were measured before intervention (basal), on 30 days (one month) and on 60 days (2 months) of intervention. Changes in means of homocysteine concentrations for placebo and vitamin D group over time showed significant difference on 30 and 60 days of intervention. Mean comparisons of homocysteine concentrations and standard error of the means before and after intervention showed statistical significant decrease in homocysteine concentrations among vitamin D group.

Conditions

Interventions

TypeNameDescription
DRUGVit D50,000 IU
OTHERPlacebo

Timeline

Start date
2016-04-01
Primary completion
2016-08-30
Completion
2016-10-30
First posted
2017-10-16
Last updated
2017-10-16

Locations

1 site across 1 country: Jordan

Source: ClinicalTrials.gov record NCT03310307. Inclusion in this directory is not an endorsement.

Vitamin D3 Treatment and Homocysteine Concentrations Among Overweight Reproductive Women (NCT03310307) · Clinical Trials Directory