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A Study of Tomato Products and Disease Risk (TOM)

Primary Purpose

Inflammation

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tomato
Non-tomato
Sponsored by
Clinical Nutrition Research Center, Illinois Institute of Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Inflammation focused on measuring Tomato, Nutrition

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Male and female
  • Between ages of 18-65
  • BMI between 19 and 24 and hsCRP < 1mg/L
  • BMI between 25 and 35 and hsCRP > 2.5mg/L
  • No clinical evidence of cardiovascular, respiratory, renal, GI or hepatic disease

Exclusion Criteria:

  • Pregnant and/or lactating
  • allergies or intolerances to foods consumed in the study
  • fasting blood glucose > 110mg/dL
  • taking OTC antioxidant supplements, prescription meds that may interfere with study endpoints
  • unusual dietary habits
  • actively trying to lose or gain weight
  • addicted to drugs or alcohol
  • medically documented psychiatric or neurological disturbances
  • smoker (past smoker allowed if cessation > 2 years)

Sites / Locations

  • Clinical Nutrition Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Tomato

Non-Tomato

Arm Description

Tomato with high carb/fat meal

Non-tomato with high carb/fat meal

Outcomes

Primary Outcome Measures

IL-6 Concentrations

Secondary Outcome Measures

Full Information

First Posted
August 26, 2009
Last Updated
February 3, 2017
Sponsor
Clinical Nutrition Research Center, Illinois Institute of Technology
Collaborators
Tomato Products Wellness Council
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1. Study Identification

Unique Protocol Identification Number
NCT00966550
Brief Title
A Study of Tomato Products and Disease Risk
Acronym
TOM
Official Title
Tomato Products and Postprandial Oxidation and Inflammation: a Clinical Trial in Healthy Weight Men and Women
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
February 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Clinical Nutrition Research Center, Illinois Institute of Technology
Collaborators
Tomato Products Wellness Council

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to test whether certain compounds in tomatoes will help reduce factors in the subject's blood associated with disease risk. The investigators want to know if the tomato-associated compounds will lower or improve the status of these factors, like cholesterol and inflammation. In this research study, the subject will be asked to consume high fat test meals on two separate occasions. The investigators want to see how the subject's body responds to a standard high fat meal, one meal with tomato products and one meal without tomato products. The investigators will measure the subject's blood throughout the study period to determine if consumption of tomato products reduces factors in their blood associated with disease risk.
Detailed Description
This study will take three weeks at most, and require one initial screening visit lasting approximately 45 minutes and two study visits each lasting approximately 6 - 8 hours. The investigators are looking for healthy, non-smoking male and female volunteers between the ages of 18 - 65, with no medical history of diabetics, heart, lung, kidney, stomach, or liver disease. The initial screening visit will determine subject' eligibility through height, weight and waist circumference measurements, blood glucose (finger prick) test and a fasting screening blood draw. There will be no compensation for the screening visit, other than transportation costs. If subject qualify, subject will continue to the two study visits. Each visit will require subject to have blood drawn several times during subject' study visit (total amount of blood equal to approximately 1 ½ tablespoons). To make this process more tolerable, a registered nurse will place a catheter (similar to what happens when you give blood) into subject's vein for ease in drawing blood. After the catheter placement and the first blood draw, subject will be asked to eat the test meal (tomato or non-tomato meal) and then subject will continue to have blood taken at specific time points for the next 6 hours. The investigators will also do an ultrasound on subject's arm to measure blood flow both before eating and midway through the 6 - hour study visit. The investigators will ask that subject not consume tomatoes or tomato products during the course of the study and record all food and beverages consumed on certain days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammation
Keywords
Tomato, Nutrition

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tomato
Arm Type
Active Comparator
Arm Description
Tomato with high carb/fat meal
Arm Title
Non-Tomato
Arm Type
Placebo Comparator
Arm Description
Non-tomato with high carb/fat meal
Intervention Type
Other
Intervention Name(s)
Tomato
Other Intervention Name(s)
Active Comparator
Intervention Description
Tomato with high carb/fat meal
Intervention Type
Other
Intervention Name(s)
Non-tomato
Other Intervention Name(s)
Placebo Comparator
Intervention Description
Non-tomato with high carb/fat meal
Primary Outcome Measure Information:
Title
IL-6 Concentrations
Time Frame
6 hour postprandial study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male and female Between ages of 18-65 BMI between 19 and 24 and hsCRP < 1mg/L BMI between 25 and 35 and hsCRP > 2.5mg/L No clinical evidence of cardiovascular, respiratory, renal, GI or hepatic disease Exclusion Criteria: Pregnant and/or lactating allergies or intolerances to foods consumed in the study fasting blood glucose > 110mg/dL taking OTC antioxidant supplements, prescription meds that may interfere with study endpoints unusual dietary habits actively trying to lose or gain weight addicted to drugs or alcohol medically documented psychiatric or neurological disturbances smoker (past smoker allowed if cessation > 2 years)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Britt Burton-Freeman, MS, PhD
Organizational Affiliation
Clinical Nutrition Research Center, Illinois Institute of Technology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Indika Edirisinghe, PhD
Organizational Affiliation
Clinical Nutrition Research Center, Illinois Institute of Technology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Nutrition Research Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60616
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22331646
Citation
Burton-Freeman B, Talbot J, Park E, Krishnankutty S, Edirisinghe I. Protective activity of processed tomato products on postprandial oxidation and inflammation: a clinical trial in healthy weight men and women. Mol Nutr Food Res. 2012 Apr;56(4):622-31. doi: 10.1002/mnfr.201100649. Epub 2012 Feb 14.
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A Study of Tomato Products and Disease Risk

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