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Study About High Fat Meal and Postprandial Lipemia

Evaluating the Effect of Lipid Overload in Endothelial Function and Microvascular Reactivity in Young Obese Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01692327
Enrollment
60
Registered
2012-09-25
Start date
2012-09-30
Completion date
2014-07-31
Last updated
2014-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

glucose intolerance (20), Control (20)

Brief summary

The hypothesis of the proposed project is that after a fat overload, the postprandial response is different in both groups, suggesting that the LPP will present the most significant damage in endothelial vasomotion in obese individuals, especially those with GI and T2DM. After the fat overload, we hypothesized that there will be a worsening of endothelial function and microvascular reactivity in OB/DM2 and OB group compared to C, but also find lower concentrations of incretins in OB/DM2 group compared to other groups. These hypotheses may be confirmed by techniques for evaluating microvascular function, the use of DFT skin for vasomotion evaluation and finally analysis of analytes through metabolic and cardiovascular read by Multiplex kit.

Detailed description

Will be recruited 60 women aged 19-40 years, with a diagnosis of obesity (BMI ≥ 30 kg/m2) treated at the obesity clinic at the State University of Rio de Janeiro (UERJ)at Brazil. Microcirculation parameters and blood tests will be assessed at baseline and after this, the women will receive a high-fat meal containing croissant, salami, whole milk and cheddar cheese. After 30, 60, 120 and 180 minutes this meal the microcirculation will be evaluated as well as blood collection.

Interventions

DIETARY_SUPPLEMENTHigh fat meal

Sponsors

Rio de Janeiro State University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* all patients should have obesity class I (BMI between 30 and 35kg/m2); * Submit diabetes mellitus without further treatment or be obese non-diabetic or glucose intolerant; * Presenting the age between 19 to 40 years. * Waist circumference\> 80 cm (IDF)

Exclusion criteria

* Renal disease, coronary or peripheral vascular, hematologic or hepatic impairment; * Presence of dyslipidemia; * smokers; * Significant loss of body weight six months prior to the study.

Design outcomes

Primary

MeasureTime frame
Microvascular functionup to 180 minutes after high fat meal

Secondary

MeasureTime frameDescription
incretins hormonesbasal, 30, 60, 120,180 minutes after high fat mealWe will assess incretins hormones by multiplex

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026