Diurnal Triglyceridemia in Relation to Alcohol Intake

February 5, 2013 updated by: Ana Torres do Rego, Sint Franciscus Gasthuis

Observational Study of Diurnal Triglyceridemia in Relation to Alcohol Intake

The purpose of this study is to determine the impact of alcohol consumption in diurnal triglyceridemia in a free living situation.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

273

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Netherlands
      • Rotterdam, Netherlands, 10900
        • Sint Franciscus Gasthuis
      • Utrecht, Netherlands
        • Utrecht University Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Subjects were healthy volunteers or patients with hyperlipidemia or a known medical history of cardiovascular diseases, type 2 diabetes mellitus participating in several clinical studies with the same protocol, aimed to investigate factors influencing postprandial lipemia

Description

Inclusion Criteria:

  • Healthy volunteers

Patients with:

  • Hyperlipidemia
  • Type 2 Diabetes Mellitus
  • Cardiovascular diseases

Exclusion Criteria:

  • Renal disease
  • Liver disease
  • Thyroid disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
General population
Healthy volunteers,patients with hyperlipidemia,a known medical history of cardiovascular diseases or type 2 diabetes mellitus.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Determination of diurnal triglyceridemia depend on alcohol intake
Time Frame: For 3 days.
Capillary triglyceridemia was measured by a triglyceride testing device on six fixed time-points.
For 3 days.

Secondary Outcome Measures

Outcome Measure
Time Frame
Gender differences in diurnal triglyceridemia by alcohol consumption
Time Frame: For 3 days
For 3 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sint Franciscus Gasthuis

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Primary Completion (Actual)

December 1, 2005

Study Registration Dates

First Submitted

January 29, 2013

First Submitted That Met QC Criteria

February 5, 2013

First Posted (Estimate)

February 8, 2013

Study Record Updates

Last Update Posted (Estimate)

February 8, 2013

Last Update Submitted That Met QC Criteria

February 5, 2013

Last Verified

February 1, 2013

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AlcoholTG_SFG_2013

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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