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Completed

NCT Number: NCT01786421

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.

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Key information

Conditions

Healthy Subjects Cardiovascular Diseases Diabetes Mellitus Diabetes Mellitus, Type 2 Dyslipidemias Endocrine System Diseases Glucose Metabolism Disorders Hyperlipidemias Lipid Metabolism Disorders Metabolic Diseases Nutritional and Metabolic Diseases Type 2 Diabetes Mellitus

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Sint Franciscus Gasthuis, Rotterdam, Netherlands

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy volunteers

Patients with:

  • Hyperlipidemia
  • Type 2 Diabetes Mellitus
  • Cardiovascular diseases

Exclusion criteria

  • Renal disease
  • Liver disease
  • Thyroid disease

Treatment and study plan

Primary outcomes

  1. 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.

Secondary outcomes

  1. Gender differences in diurnal triglyceridemia by alcohol consumption

    Time frame: For 3 days

Sponsors and collaborators

Lead sponsor

Sint Franciscus Gasthuis

Other

Registry information

Official study title

Observational Study of Diurnal Triglyceridemia in Relation to Alcohol Intake

Important dates

Primary completion
2005
First posted
Feb 8, 2013
Registry last updated
Feb 8, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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