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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | vitamin D3 | vitamin D3 (cholecalciferol) 800 IU QD |
| DIETARY_SUPPLEMENT | calcium | calcium 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.