Overview
Efficacy Of Ergocalciferol In Adults According To BMI
Status:
Terminated
Terminated
Trial end date:
2017-04-01
2017-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Vitamin D insufficiency is an increasing trend in the United States. According to the NHANES data collection there was a near doubling of patients with vitamin D deficiency in 10 years. Vitamin D deficiency is associated with several adverse outcomes such as increased fractures, certain microbial diseases, cardiovascular diseases, and metabolic dysfunction. The increasing prevalence of vitamin D deficiency has been attributed to the increasing prevalence of obesity. Several studies have shown that obese patients have lower 25-OH vitamin D (25-OHD) levels compared to nonobese patients and obese patients require more vitamin D compared to nonobese patients. The most commonly prescribed medication to replete vitamin D deficiency is oral ergocalciferol. To date, no prospective trials have been published to evaluate a standard protocol in the treatment of vitamin D insufficiency in adults.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Walter Reed National Military Medical CenterTreatments:
Ergocalciferols
Vitamin D
Criteria
Inclusion Criteria:- Study subjects have to be between the ages of 18 to 65 with a serum 25OHD level less
than 20 ng/ml.
Exclusion Criteria:
- Participants will be excluded if they have any of the following:
1. Due to the inaccuracies of BMI in patients with increased muscle mass, in group
with a BMI 25-35: men with a waist circumference < 90 cm ; women < 80 cm
2. Chronic liver disease defined by any clinical or a history of serum AST or ALT >
2 times ULN
3. Kidney disease defined as a GFR <60 ml/min
4. Sarcoidosis
5. Any known malignancy
6. Known malabsorption disorder to include inflammatory bowel disease, celiac
disease, cystic fibrosis, history of gastric bypass
7. Primary hyperparathyroidism or hypercalcemia,
8. Patients that are pregnant or considering pregnancy.
9. Patients taking certain medications such as glucocorticoids, anti-seizure
medications such has phenobarbital or phenytoin or patients taking antiviral
medications for HIV as these are known to cause vitamin D deficiency
10. Individuals excluded from having a DXA scan
Study participants will be excluded from having a DXA scan if any of the following:
1. Any amputation of a extremity including toes
2. If they have a pacemaker, automatic defibrillator, coronary stents or metal suture
material in the heart
3. If they have artificial joints, pins, plate or any other type of metal objects
4. If they have received contrast material such as barium in the past 7 days
5. If they have had a nuclear medicine study in the past 3 days