Lactate Metabolism After an Endotoxin Challenge in Healthy Humans
Effects of an Acute Administration of Bacterial Endotoxin on Whole Body and Regional Lactate Metabolism in Healthy Male Volunteers
Sepsis is characterized by hyperlactatemia, the severity of which is proportionate with sepsis severity. The pathophysiological mechanisms (increased lactate production vs decreased lactate utilization; tissues involved in sepsis-induced lactate production) remain largely unknown.
In this study, the investigators will assess whole body and regional metabolism in healthy young male subjects on two occasions, once after administration of an intravenous bacterial endotoxin challenge, and once without intervention.
In one group of subjects, whole body lactate metabolism will be measured over 10 hours after the endotoxin challenge
- Energy expenditure and net substrate oxidation rates (indirect calorimetry)
- Lactate kinetics (measured by means of a continuous, exogenous sodium lactate infusion)
- Glucose kinetics (measured with 6,6 d2 glucose)
- Hemodynamic parameters and body temperature
- Blood clinical chemistry In one group of subjects, whole body lactate metabolism will be measured over 10 hours after the endotoxin challenge
- Energy expenditure and net substrate oxidation rates (indirect calorimetry)
- Lactate kinetics (measured by means of a continuous, exogenous sodium lactate infusion)
- Glucose kinetics (measured with 6,6 d2 glucose)
- Hemodynamic parameters and body temperature
- Blood clinical chemistry
In a second group of subjects, regional muscle lactate metabolism will be measured over 10 hours after the endotoxin challenge by means of muscle microdialysis
調査の概要
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
-
-
Vaud
-
Lausanne、Vaud、スイス、CH-1011
- Centre Hospitalier Universitaire Vaudois
-
-
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:
- gender male
- body mass index (BMI) < 25 kg/m2
- absence of known disease
Exclusion Criteria:
- any known pathology
- abnormal cardio-pulmonary and hemodynamic status
- electrocardiographic alterations
- history of allergy
- current medications
- drug abuse
- consumption of more than 20g/day alcohol
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：ランダム化
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：study 1a
whole body lactate production after bacterial endotoxin challenge
|
iv administration of 2ng/kg bacterial endotoxin
|
|
介入なし：study 1b
basal whole body lactate production
|
|
|
実験的：study 2a
muscle lactate concentration after bacterial endotoxin challenge
|
iv administration of 2ng/kg bacterial endotoxin
|
|
介入なし：study 2b
basal muscle lactate concentrations
|
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 |
|---|---|---|
|
Whole body lactate production
時間枠：single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
Whole body lactate clearance will be measured by measuring the increase in blood lactate at steady state during a conrtinuous exogenous sodium lactate infusion. Lactate production will be calculated as the product of lactate clearance times per-infusion blood lactate concentration |
single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
|
skeletal muscle lactate concentration
時間枠：single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
interstitial muscle measured by means of in vivo microdialysis ; calculation of muscle-blood lactate gradient
|
single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
whole body energy expenditure
時間枠：single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
open circuit indirect calorimetry (hood)
|
single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
|
body temperature
時間枠：single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
single bacterial endotoxin administration; measurements over 6.5 hours following administration
|
協力者と研究者
スポンサー
捜査官
- 主任研究者：René Chiolero, MD、Centre Hospitalier Universitaire Vaudois
出版物と役立つリンク
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
- Lsne-128/01
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。