Overview
Evaluating Vitamin D3 Supplement on Post-Op Outcomes
Status:
Active, not recruiting
Active, not recruiting
Trial end date:
2022-01-01
2022-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of this study is to determine if vitamin D supplementation is associated with differences in short-term recovery in patients following total knee arthroplasty compared to patients who do not receive supplementation. If so, vitamin D supplementation has the potential to become widely incorporated into the routine care for patients undergoing knee replacements.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Rush University Medical CenterTreatments:
Cholecalciferol
Ergocalciferols
Vitamin D
Vitamins
Criteria
Inclusion Criteria:- Any patient undergoing primary total knee arthroplasty for osteoarthritis
- Age ≥ 18 years old
- Willingness to undergo randomization and return for all scheduled visits
Exclusion Criteria:
- Age > 80 years old
- American Society of Anesthesiologists (ASA) Score ≥ 4
- Other supplemental vitamin D or Calcium use including their analogs: ergocalciferol,
calcitriol, dihydrotachysterol, and paricalcitol
- Current cancer
- Malabsorption syndromes
- Inability to take medications orally
- Renal impairment defined as a glomerular filtration rate (GFR) < 30 mL/minute or
creatinine >1.3 mg/dL
- History of hypercalcemia defined as albumin-corrected hypercalcemia >12 mg/dL