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Diurnal Triglyceridemia in Relation to Alcohol Intake

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01786421
First Posted: February 8, 2013
Last Update Posted: February 8, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Ana Torres do Rego, Sint Franciscus Gasthuis
January 29, 2013
February 8, 2013
February 8, 2013
Not Provided
December 2005   (Final data collection date for primary outcome measure)
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.
Same as current
No Changes Posted
Gender differences in diurnal triglyceridemia by alcohol consumption [ Time Frame: For 3 days ]
Same as current
Not Provided
Not Provided
 
Diurnal Triglyceridemia in Relation to Alcohol Intake
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.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Retrospective
Not Provided
Not Provided
Probability Sample
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
  • Healthy Subjects
  • Hyperlipidemias
  • Type 2 Diabetes Mellitus
  • Cardiovascular Diseases
Not Provided
General population
Healthy volunteers,patients with hyperlipidemia,a known medical history of cardiovascular diseases or type 2 diabetes mellitus.
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
273
Not Provided
December 2005   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Healthy volunteers

Patients with:

  • Hyperlipidemia
  • Type 2 Diabetes Mellitus
  • Cardiovascular diseases

Exclusion Criteria:

  • Renal disease
  • Liver disease
  • Thyroid disease
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Senior)
Yes
Contact information is only displayed when the study is recruiting subjects
Netherlands
 
 
NCT01786421
AlcoholTG_SFG_2013
No
Not Provided
Not Provided
Ana Torres do Rego, Sint Franciscus Gasthuis
Sint Franciscus Gasthuis
Not Provided
Not Provided
Sint Franciscus Gasthuis
February 2013