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Postoperative Vitamin Supplementation in Morbidly Obese Patient (VITAAL Study)

NCT01609387 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2016-05-03

No results posted yet for this study

Summary

This study is a double blind randomized controlled trial.

Conditions

Interventions

DIETARY_SUPPLEMENT

Fit For me

DIETARY_SUPPLEMENT

Davitamon

Sponsors & Collaborators

  • Rijnstate Hospital

    lead OTHER

Principal Investigators

  • Frits Berends, MD,PhD · Rijnstate Arnhem

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2015-10-31
Completion
2015-12-31

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01609387 on ClinicalTrials.gov