Clinical Trials Directory

Trials / Completed

CompletedNCT05023122

The Effect of Oral Vitamin D Supplements on Fusion Outcome in Patients Receiving Elective Lumbar Spinal Fusion

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Show Chwan Memorial Hospital · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The process of bony fusion is a dynamic bone remodeling process and a variety of risk factors have been identified to contribute to pseudoarthrosis.Vitamin D deficiency has been reported to be associated with more pseudoarthrosis, prolonged time to fusion, and poorer spine function and quality of life after spinal fusion.However, as the review article presented, it lacks high-quality evidence to investigate the role of vitamin D supplements in spinal fusion. Therefore, this randomized controlled trial aimed to evaluate the effectiveness of oral vitamin D supplements on fusion outcomes in patients receiving elective lumbar spinal fusion.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTvitamin D3vitamin D3 (cholecalciferol) 800 IU QD
DIETARY_SUPPLEMENTcalciumcalcium citrate 600 mg QD

Timeline

Start date
2016-01-01
Primary completion
2017-12-31
Completion
2018-12-31
First posted
2021-08-26
Last updated
2021-08-26

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT05023122. Inclusion in this directory is not an endorsement.