Obesity Clinical Trial
Official title:
Study to Evaluate the Pharmacokinetics of Vitamin D (Cholecalciferol) in Patients Undergoing Obesity Surgery in a Deficit Situation and After Standardization
Set the pattern of vitamin D supplementation in obese patients undergoing bariatric surgery
in deficit of vitamin D.
Patients receive a single oral dose of vitamin D, during the 28 days will be done a kinetic
curve. Then and over the next 3 months, levels are normalized. Once normalized, will be
administered another single oral dose to a second pharmacokinetic evaluation.
The study is conducted in obese patients undergoing bariatric surgery (for bypass or sleeve
gastrectomy) in deficit of vitamin D.
Will include a total of 44 patients, 22 from each type of surgery. Patients receive a single
oral dose of vitamin D of 50,000 IU. During the 28 days after administration of vitamin D
will be done a kinetic curve determining plasma levels of vitamin D on 15 occasions. Then
and over the next 3 months, levels are normalized by providing a daily oral dose for each
patient. Once levels are normalized, will be administered another single oral dose of 50,000
IU vitamin D and proceed to a second pharmacokinetic evaluation determining plasma levels 15
times.
Patient follow up is approximately 36 weeks. Patients go to the screening visit, baseline
visit and visits on days 1, 2, 3, 14 and 28 days after each pharmacokinetic evaluation.
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Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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