Clinical Trials Directory

Trials / Completed

CompletedNCT01609387

Postoperative Vitamin Supplementation in Morbidly Obese Patient (VITAAL Study)

Postoperative Vitamin Supplementation in Morbidly Obese Patient

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
300 (actual)
Sponsor
Rijnstate Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study is a double blind randomized controlled trial.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTFit For me
DIETARY_SUPPLEMENTDavitamon

Timeline

Start date
2011-07-01
Primary completion
2015-10-01
Completion
2015-12-01
First posted
2012-06-01
Last updated
2016-05-03

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01609387. Inclusion in this directory is not an endorsement.