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Oral Vitamin D Supplementation Prevent Peritoneal Dialysis-related Peritonitis — VD-PD  

Vitamin D Deficiency Clinical Trial

Official title:
The Effects of Oral Vitamin D Supplementation on the Prevention of Peritoneal Dialysis-related Peritonitis, a Multicenter Randomized Controlled Trial

Clinical Trial Summary

This is a multicenter randomized, placebo-controlled trial of Vitamin D supplementation in patients on peritoneal dialysis to determine whether oral administration of vitamin D3 after curing an episode of peritonitis could reduce the risk of subsequent peritoneal dialysis-related peritonitis.

Clinical Trial Description

176 eligible patients on PD at one month after being cured from an episode of peritonitis will be enrolled and randomized into two groups, including the intervention group administered Cholecalciferol (produced by Xymogen Company) 4000 U (2 capsules) per day, and the control group administered placebo 2 capsules per day. All participants will be followed for 24 months, or till the occurrence of death, permanently transfer to hemodialysis, loss of follow-up, or withdrawal from the study, whichever comes first. The primary outcome is the occurrence of subsequent peritonitis. The study aims to identify whether oral administration of vitamin D3 after curing an episode of peritonitis could reduce the risk of subsequent peritoneal dialysis-related peritonitis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05860270
Study type Interventional
Source Peking University First Hospital
Contact Jie Dong, Professor
Phone 13911841538
Email jie.dong@bjmu.edu.cn
Status Recruiting
Phase Phase 4
Start date June 15, 2023
Completion date May 31, 2026
View Details
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