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Efficacy Of Ergocalciferol In Adults According To BMI

Efficacy Of Ergocalciferol In Adults According To BMI

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02435771
Enrollment
44
Registered
2015-05-06
Start date
2011-07-31
Completion date
2017-04-30
Last updated
2017-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Vitamin D Deficiency

Brief 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.

Interventions

Treatment 1- 400,000 IU

Sponsors

Walter Reed National Military Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
serum 25-hydroxy-vitamin D level12 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026