The Effect of Dietary Fat Modification on Risk Factors Associated With the Metabolic Syndrome

NCT00429195 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 480

Last updated 2013-01-21

No results posted yet for this study

Summary

The LIPGENE Human Dietary Intervention Study, multi-centre, trans -European, single-blinded, randomised, controlled trial with two principal aims. Firstly to determine the relative efficacy of reducing dietary SFA consumption, by altering quality of dietary fat and reducing the quantity of dietary fat, on metabolic and molecular risk factors of the metabolic syndrome. Secondly to determine if common genetic polymorphisms affect an individual's responsiveness to dietary therapy.

Conditions

  • Metabolic Syndrome

Interventions

BEHAVIORAL

Dietary Fatty Acid Modification

Sponsors & Collaborators

  • University of Reading

    collaborator OTHER
  • University of Oslo

    collaborator OTHER
  • Institut National de la Santé Et de la Recherche Médicale, France

    collaborator OTHER_GOV
  • Maastricht University Medical Center

    collaborator OTHER
  • Universidad Nacional de Córdoba

    collaborator OTHER
  • Jagiellonian University

    collaborator OTHER
  • Uppsala University

    collaborator OTHER
  • University College Dublin

    lead OTHER

Principal Investigators

  • Helen M Roche, PhD · University of Dublin, Trinity College

  • Christine Williams, PhD · University of Reading

  • Christian Drevon, MD · University of Oslo

  • Denis Larion, PhD · INSERM, Marseille

  • Wim Saris, PhD · Maastricht University

  • Jose Lopez Miranda, MD, PhD · Universidad de Córdoba

  • Aldona Dembinska-Kiec, MD · The Jagiellonian University Medical College

  • Bengt Vessby, MD · Uppsala University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
35 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2004-02-29
Completion
2007-01-31

Countries

  • Ireland

Study Locations

More Related Trials

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 NCT00429195 on ClinicalTrials.gov