Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Endothelial Dysfunction Induced by Postprandial Lipemia
This study has been completed.
Sponsored by: Norwegian University of Science and Technology
Information provided by: Norwegian University of Science and Technology
ClinicalTrials.gov Identifier: NCT00660491
  Purpose

Postprandial lipemia and exercise oppose each other in terms of cardiovascular risk, however the mechanism of their interaction is not well understood.

Therefore we want to study vascular function, as assessed by brachial artery (BA) flow mediated dilation (FMD), in healthy men before and after a high fat meal (HFM) preceded (16-18 hrs) by rest, a single bout of continuous moderate intensity exercise (CME), and high intensity interval exercise (HIIE).


Condition Intervention Phase
Blood Lipids
Other: exercise training
Phase II

MedlinePlus related topics: Exercise and Physical Fitness
Drug Information available for: Lipids
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver), Crossover Assignment
Official Title: Endothelial Dysfunction Induced by Postprandial Lipemia: Complete Protection Afforded by High Intensity Aerobic Interval Exercise

Further study details as provided by Norwegian University of Science and Technology:

Primary Outcome Measures:
  • Flow mediated dilatation [ Time Frame: baseline, post exercise, 30min, 2hour, 4hour post exercise ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • blood lipid profile [ Time Frame: same as flow mediated dilatation ] [ Designated as safety issue: No ]

Estimated Enrollment: 8
Study Start Date: January 2008
Study Completion Date: October 2008
Primary Completion Date: September 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: No Intervention
Control
2: No Intervention
moderate exercise training group
3: Experimental
high intensity exercise group
Other: exercise training
moderate intensity exercise group, and high intensity exercise group

  Eligibility

Ages Eligible for Study:   20 Years to 40 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • male, 20-40years, BMI between 25 and 30, resident in Trondheim.

Exclusion Criteria:

  • unstable angina, CHD, heart failure,
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00660491

Locations
Norway
NTNU
Trondheim, Norway, 7489
Sponsors and Collaborators
Norwegian University of Science and Technology
Investigators
Study Chair: Ulrik Wisloff, Professor NTNU
  More Information

Publications indexed to this study:
Responsible Party: NTNU ( Ulrik Wisloff )
Study ID Numbers: Exercise, Food and Endothelium
Study First Received: April 15, 2008
Last Updated: November 3, 2008
ClinicalTrials.gov Identifier: NCT00660491  
Health Authority: Norway: The National Committees for Research Ethics in Norway

Keywords provided by Norwegian University of Science and Technology:
flow mediated dilatation
maximal oxygen uptake
blood lipid

Study placed in the following topic categories:
Hyperlipidemias
Dilatation, Pathologic

ClinicalTrials.gov processed this record on January 15, 2009