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Search / Trial NCT03534674

Vitamin D3 Supplementation for AlloHSCT-RCT

Launched by UNIVERSITY OF BRITISH COLUMBIA · May 11, 2018

Trial Information

Current as of May 16, 2025

Unknown status

Keywords

ClinConnect Summary

This is a randomized non-blinded single centre prospective clinical trial designed to validate whether a single oral loading dose of 100,000 IU vitamin D3 prior to allogeneic hematopoietic stem cell transplant (aHSCT) can achieve optimal 25 hydroxy-vitamin D3(25-OH-D3) levels (\>75nmol/L) at one month post aHSCT, and maintain adequate levels for at least three months, compared to our standard practice of 2000 IU vitamin D3 daily.

84 patients will be enrolled. Following completion of all baseline data collection, participants will be randomized 1:1 to the intervention group or the control g...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Patients undergoing allogeneic stem cell transplantation at the Leukemia/BMT Program of British Columbia.
  • 2. Age greater than or equal to 18 years.
  • 3. Able to provide written informed consent.
  • Exclusion Criteria:
  • 1. Hypercalcemia, hypervitaminosis D, or allergic/ sensitive to vitamin D.
  • 2. Not meeting eligibility criteria to proceed with allogeneic stem cell transplantation as per the Leukemia/BMT Program of BC.

About University Of British Columbia

The University of British Columbia (UBC) is a leading research institution located in Vancouver, Canada, renowned for its commitment to advancing health sciences through innovative research and education. As a prominent clinical trial sponsor, UBC leverages its interdisciplinary expertise and state-of-the-art facilities to conduct rigorous clinical studies aimed at improving patient outcomes across various medical fields. The university fosters collaborations with healthcare professionals, industry partners, and community stakeholders to translate research findings into practical applications, thereby contributing to the global advancement of medicine and public health.

Locations

Vancouver, British Columbia, Canada

Patients applied

0 patients applied

Trial Officials

Raewyn Broady, MBChB

Principal Investigator

British Columbia Cancer Agency

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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