Burger and Beetroot Study - Lipid Oxidation Study (BABS)
Lipid Oxidation of Ready Meals: Reformulation With Antioxidant Phytochemicals
調査の概要
詳細な説明
Many of these lipid oxidation products such as malondialdehyde are known to be genotoxic and potentially detrimental to health. Consequently the aim of this study is to assess whether consumption of "ready meals" rich in certain fats leads to a post-prandial increase in lipid oxidation products in plasma and whether this can be ameliorated by reformulating the meals with natural extracts rich in phytochemicals with potential antioxidant activity in the stomach.
Diet design requirements:
The basic "ready meal" is a turkey burger consisting of
- 50% fat
- 20% protein
- 30% carbohydrate.
However, there are four experimental forms of the burger.
- The fat is unsaturated (stripped corn oil)
- The fat is saturated (lard)
- The fat is unsaturated and the diet also contains a beetroot extract at a concentration of 10g/100g.
- The fat is saturated and the diet also contains a beetroot extract at a concentration of 10g/100g.
Beetroot (http://www.kanegrade.com/powders.htm) has been selected for the burger reformulation as it is a Scottish product rich in phytochemicals with potential antioxidant efficacy. An additional benefit may a blood pressure lowering effect. Initial taste tests indicate acceptable palatability.
All other components of the burger are formulated to be as similar as possible.
Fatty acid profiles and the "basic eight" used on food labels will be determined on the diets. Susceptibility of the diets to oxidise will be assessed using RANCIMAT.
Ready Meal Intervention:
This will be a latin square format whereby each volunteer consumes 4 treatments on separate occasions. This is a powerful design to assess whether incorporation of phytochemicals from Scottish products improves the health benefits of processed food as each volunteer acts as his/her own control. Volunteers will be randomly allocated to four groups
- Treatment A High polyunsaturated (PUFA) ready meal (ie. burger)
- Treatment B High saturated (SFA) fat ready meal
- Treatment C High PUFA ready meal incorporating food extract
- Treatment D High SFA ready meal incorporating food extract
There will be a washout period of at least 7 days between each treatment.
Volunteers:
Healthy volunteers aged 21 to 60 years will be recruited and attend HNU having fasted from 22.00h the previous evening on four test days. On arrival, they will be asked to provide a urine sample. The volunteers will then have a cannula inserted by a trained nurse and an initial baseline blood sample will be taken (volume 10 ml). The subjects will then be asked to consume the assigned breakfast within a 15 minute period. Water will be provided. Volunteers will then be requested to provide 10ml blood samples at 1h, 2h, 4h and 6h and 24 hrs. A 24 hr urine sample also will be obtained, starting the day of the test day. Blood pressure will be recorded at each time point.
Volunteers will not be included if they
- Are taking any medicines prescribed by their GP
- Have a known allergy to beetroot
- Are vegetarian or vegan
- Regularly take nutritional supplements
- Have given a large blood donation in last three months
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
-
Scotland
-
Aberdeen、Scotland、イギリス、AB21 9SB
- Human Nutrition Unit, Rowett Institute of Nutrition and Health
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- No diagnosed clinical condition
Exclusion Criteria:
Are taking any medicines prescribed by their GP Have a known allergy to beetroot Are vegan Regularly take nutritional supplements Have given a large blood donation in last three months
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:基礎科学
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Burger and Beetroot Study
|
50% fat, 10% beetroot extract
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Lipid peroxides
時間枠:up to 24 hours
|
Indices of oxidised lipids in plasma
|
up to 24 hours
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Blood pressure
時間枠:up to 24 hours
|
Systolic and diastolic blood pressure
|
up to 24 hours
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Garry G Duthie, PhD、University of Aberdeen
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- HNU 2000
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。