The Effect of Meat and Food Drived Polyphenols on Oxidize LDL Level
This study has been completed.
Sponsor:
Hadassah Medical Organization
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01389492
First received: July 3, 2011
Last updated: July 6, 2011
Last verified: October 2009
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The postprandial increase in MDA level following meat meal could cause modification to LDL particles in healthy volunteers. Co-consumption of food drived polyphenols with the meat will result in a significant decrease in LDL modification.
| Condition | Intervention |
|---|---|
|
Healthy |
Other: frozen meat cutlets meal Other: meat meals |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Bio-availability Study Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Basic Science |
| Official Title: | Nutritional Study:The Effect of Meat and Food Drived Polyphenols on Oxidize LDL Level |
Further study details as provided by Hadassah Medical Organization:
Primary Outcome Measures:
- Change in plasma MDA levels following meat meal [ Time Frame: Fasting before meal and 3, and 6 h postprandial, and fasting levels ] [ Designated as safety issue: No ]After an overnight fast baseline (0 h) fasting blood sample (10 ml) was collected in EDTA-treated tubes. The subjects then ate a test meal within 30 min. Blood samples (10 ml) were drawn 3 and 6 h after the meal was eaten. Serum was separated from whole blood by centrifugation (910 g, 15 min), and MDA was evaluated by HPLC in plasma samples
- Changes in MDA concentration on LDL fraction following meat meals [ Time Frame: Fasting, before meal was eaten, 3 h following meal, at day 4, 3 h following meal consumption, and day 5 following over nigth fast ] [ Designated as safety issue: No ]Subject consumed the test meals for 4 days. Day 1, (0 h) fasting blood sample (10 ml) was collected in EDTA-treated tubes. The sbjects then ate a test meal within 30 min. Blood samples (10 ml) were drawn 3 h after the meal was eaten. Blood was collected at day 4, 3 h after the meal was eaten, at the morning of day 5.Plasma LDL was isolated using a single discontinuous density gradient ultracentrifugation. The protein concentration was determined based on the method of Bradford. MDA concentration was evaluated by HPLC.
| Enrollment: | 14 |
| Study Start Date: | October 2010 |
| Study Completion Date: | May 2011 |
| Primary Completion Date: | February 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
frozen meat
250 g of frozen meat meal for 4 days
|
Other: frozen meat cutlets meal
250 g of meat cutlets
Other: meat meals
250 g of meat meal for 4 days
|
|
frozen meat and wine
250 g of frozen meat and red wine for 4 days
|
Other: frozen meat cutlets meal
250 g of meat cutlets
Other: meat meals
250 g of meat meal for 4 days
|
|
fresh meat
250 g of fresh meat meal
|
Other: frozen meat cutlets meal
250 g of meat cutlets
Other: meat meals
250 g of meat meal for 4 days
|
|
fresh meat and wine
250 g of fresh meat meal
|
Other: frozen meat cutlets meal
250 g of meat cutlets
Other: meat meals
250 g of meat meal for 4 days
|
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Healthy adults, normal BMI
Exclusion Criteria:
- Metabolic disorders
- Smokers
- Drinkers
- Taking nutritional supplement
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Dr. Daniel Schurr, Hadassah Medical Organization |
| ClinicalTrials.gov Identifier: | NCT01389492 History of Changes |
| Other Study ID Numbers: | MWPP09-HMO-CTIL |
| Study First Received: | July 3, 2011 |
| Last Updated: | July 6, 2011 |
| Health Authority: | Israel: Ministry of Health - Director General |
Keywords provided by Hadassah Medical Organization:
|
meat LDL MDA |
ClinicalTrials.gov processed this record on June 18, 2013