ClinicalTrials.Veeva

Menu

Peri-operative Vitamin D Therapy for Hepatectomy

National Taiwan University logo

National Taiwan University

Status

Not yet enrolling

Conditions

Perioperative Complication
Vitamin D Deficiency
Hepatocellular Carcinoma

Treatments

Dietary Supplement: Placebo
Dietary Supplement: Vitamin D

Study type

Interventional

Funder types

Other

Identifiers

NCT05650151
202209057RINA
2022-11-007A (Other Identifier)

Details and patient eligibility

About

The goal of this double-blind, randomized controlled trial is to test the effect of short-term and high-dose vitamin D therapy in patients undergoing hepatectomy for hepatocellular carcinoma.

Full description

Participants will receive short-term high dose of vitamin D during perioperative period.

The main questions the study aims to answer are:

  1. If vitamin D therapy benefits perioperative care
  2. If short-term high dose of vitamin D supplement is safe

Enrollment

200 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients older than 20 years
  • Patients will undergo hepatectomy for hepatocellular carcinoma.

Exclusion criteria

  • Patients with hypercalcemia, hyperparathyroidism, sarcoidosis, multiple myeloma

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

200 participants in 2 patient groups, including a placebo group

Vitamin D group
Experimental group
Treatment:
Dietary Supplement: Vitamin D
Control group
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

0

Loading...

Central trial contact

Yin-Yi Han, PHD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems