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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02529709
Other study ID # TexasCU
Secondary ID
Status Completed
Phase N/A
First received August 14, 2015
Last updated April 19, 2016
Start date October 2015
Est. completion date April 2016

Study information

Verified date April 2016
Source Texas Christian University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if a high-protein meal leads to a better postprandial (after a meal) blood lipid profile compared to a high-monounsaturated meal.


Description:

The effect of a high-protein diet compared to a high-monounsaturated fat diet on fasting lipids is controversial (1,2), In addition, these studies did not examine the effect of a high-protein compared to a high-monounsaturated meal on postprandial lipid concentrations. Postprandial lipid responses are important to examine since they are associated with heart disease (3,4). In addition, most individuals in Western countries are in a postprandial state for majority of the day. The present study will compare the effect of a high-protein meal versus a high-monounsaturated fat meal on postprandial lipid responses.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Men and women ages 18-65 years.

Exclusion Criteria:

- Use of medications or supplements that affect lipid levels, body weight, or blood glucose,

- following a weight loss diet,

- being a vegan,

- smoking,

- heavy alcohol use,

- pregnancy,

- lactation,

- severe depression,

- eating disorders,

- presence of liver, kidney, gastrointestinal, adrenal, or untreated thyroid disease,

- diabetes,

- lactose intolerance,

- documented mal-absorption, or

- bowel surgery that affects absorption.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
High-Protein Condition
The participants will be fed a high-protein meal
High-Monounsaturated Fat Condition
The participants will be fed a high-monounsaturated fat meal

Locations

Country Name City State
United States Texas Christian University Fort Worth Texas

Sponsors (1)

Lead Sponsor Collaborator
Texas Christian University

Country where clinical trial is conducted

United States, 

References & Publications (4)

Appel LJ, Sacks FM, Carey VJ, Obarzanek E, Swain JF, Miller ER 3rd, Conlin PR, Erlinger TP, Rosner BA, Laranjo NM, Charleston J, McCarron P, Bishop LM; OmniHeart Collaborative Research Group. Effects of protein, monounsaturated fat, and carbohydrate intake on blood pressure and serum lipids: results of the OmniHeart randomized trial. JAMA. 2005 Nov 16;294(19):2455-64. — View Citation

Bansal S, Buring JE, Rifai N, Mora S, Sacks FM, Ridker PM. Fasting compared with nonfasting triglycerides and risk of cardiovascular events in women. JAMA. 2007 Jul 18;298(3):309-16. — View Citation

Luscombe-Marsh ND, Noakes M, Wittert GA, Keogh JB, Foster P, Clifton PM. Carbohydrate-restricted diets high in either monounsaturated fat or protein are equally effective at promoting fat loss and improving blood lipids. Am J Clin Nutr. 2005 Apr;81(4):762-72. — View Citation

Simons LA, Dwyer T, Simons J, Bernstein L, Mock P, Poonia NS, Balasubramaniam S, Baron D, Branson J, Morgan J, et al. Chylomicrons and chylomicron remnants in coronary artery disease: a case-control study. Atherosclerosis. 1987 May;65(1-2):181-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Blood lipid concentrations. At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary IL-6 At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary TNF-a At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary C-reactive protein At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary GLP-1 At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary Insulin At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary Glucagon At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary Glucose At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
Secondary Leptin At 0 minute before the meal begins and at 30, 60, 120, and 180 minutes after the meal begins Yes
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