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Postoperative Vitamin Supplementation in Morbidly Obese Patient (VITAAL Study)

Obesity Clinical Trial

Official title:
Postoperative Vitamin Supplementation in Morbidly Obese Patient

Clinical Trial Summary

This study is a double blind randomized controlled trial.

Clinical Trial Description

Based on evidence-based literature on vitamins and minerals, there is a cooperation of a manufacturer multivitamin specifically designed for patients with a gastric band and Roux-en-Y gastric bypass (RYGB). These preparations are the proportions adjusted so that the risk of shortages should decrease and on the other hand, excessive levels of nutrients should be avoided. Main objective of this study is to examine whether these new supplements in particular the number of deficiencies in iron, vitamin B12 and vitamin D can be reduced. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01609387
Study type Interventional
Source Rijnstate Hospital
Contact
Status Completed
Phase Phase 4
Start date July 2011
Completion date December 2015
View Details
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