Overview

Evaluating Vitamin D3 Supplement on Post-Op Outcomes

Status:
Active, not recruiting
Trial end date:
2022-01-01
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Rush University Medical Center
Treatments:
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