Oral Vitamin D Supplementation Prevent Peritoneal Dialysis-related Peritonitis

NCT05860270 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 176

Last updated 2024-08-06

No results posted yet for this study

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.

Conditions

  • Peritoneal Dialysis-associated Peritonitis
  • Vitamin D Deficiency

Interventions

DRUG

Cholecalciferol

Patients in the intervention group will receive oral cholecalciferol 4000U per day.

DRUG

Placebo

Patients in the control group will receive placebo 2 capsules per day.

Sponsors & Collaborators

  • Peking University Third Hospital

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Beijing Haidian Hospital

    collaborator OTHER
  • Peking University Shenzhen Hospital

    collaborator OTHER
  • Miyun District of Peking University First Hospital

    collaborator UNKNOWN
  • Beijing Fangshan District Hospital of Traditional Chinese Medicine

    collaborator UNKNOWN
  • Peking University International Hospital

    collaborator OTHER
  • Beijing Tsinghua Changgeng Hospital

    collaborator OTHER
  • Beijing Anzhen Hospital

    collaborator OTHER
  • Capital Medical University

    collaborator OTHER
  • Peking University First Hospital

    lead OTHER

Principal Investigators

  • Jie Dong · Peking University First Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-15
Primary Completion
2026-03-31
Completion
2026-05-31

Countries

  • China

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05860270 on ClinicalTrials.gov