高齢者の慢性静脈性下肢潰瘍の治癒に対するオメガ-3脂肪酸経口療法の影響
調査の概要
詳細な説明
CVLU の病因には、創傷床の持続性炎症に関連する多数の活性化多形核白血球 (PMN) が含まれます。 提案された研究は、魚油の生理活性成分 (エイコサペンタエン酸 - EPA + ドコサヘキサエン酸 - DHA) を含む経口栄養介入の有効性をテストして、PMN 活動を緩和し、治癒を促進することです。 この研究には、大学の 2 つの外来創傷クリニックで標準治療を受け続けている CVLU を持つ 55 歳以上の適格成人 248 人が含まれる予定です。 参加者は 2 つのグループに無作為に割り付けられます: 12 週間の EPA + DHA (1.87 g/d EPA + 1.0 g/d DHA) による毎日の経口療法またはプラセボによる毎日の経口療法。 0、4、8、および 12 週で、2 つのグループ全体で、3 つの具体的な目標が追求されます。
目的 1. 血中および CVLU 液中の EPA+DHA 由来の脂質メディエーターと炎症性サイトカインのレベルを比較します。
サブエイム 1a. 血中の PMN (好中球と単球) による炎症性サイトカイン遺伝子の発現を比較します。
目的 2. PMN 活性化 (血液、CVLU 液) と PMN 由来プロテアーゼ レベル (CVLU 液) を比較します。
目的 3. 創傷面積の減少を比較し、治癒に影響を与えることが知られている重要な要因を制御し、脂質メディエーター、サイトカイン、および PMN 活性化との関係を決定します。
サブエイム 3a. CVLU が治癒した EPA + DHA グループ内の 2 つのサブグループ間で、CVLU 再発の頻度と血中の研究変数のレベルを比較します (12 週目以降の EPA + DHA 療法とプラセボ療法の追加の 3 か月後)。
サブエイム 3b. 2 つのグループと 2 つのサブグループ間で、すべての時点での痛みの症状と、最初と最後の研究訪問時の生活の質を比較します。
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
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Ohio
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Columbus、Ohio、アメリカ、43210
- The Ohio State University College of Nursing
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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
説明
包含基準:
55歳以上の女性および男性:
- 足首と膝の間の CVLU が 4 週間以上 12 か月以内で、1 ~ 4 層の包帯による圧迫療法が処方されました。
- -足首上腕圧指数(ABPI)が0.7〜1.2;
- 対象の創傷面積が 2 ~ 60 cm2 の場合
- 英語またはスペイン語を読んで理解し、
- 同意します。
除外基準:
- 魚アレルギー;
- コルチコステロイドまたは選択的シクロオキシゲナーゼ (COX)-2 阻害剤 (例: Celebrex);非ステロイド性抗炎症薬 (NSAIDS) > 週 2 回 (例外: アスピリン 81 mg/日);
- 自己免疫疾患;
- -0週から6か月以内の化学療法;
- HbA1c > 12% の場合は糖尿病、または蜂窩織炎、露出した腱または骨を合併した潰瘍。
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:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:EPA+DHAグループ
EPA+DHA による 12 週間の毎日の経口療法 (EPA 1.87 g + DHA 1.0 g の 1 日総摂取量を提供する 3 つの不透明なソフトジェル)
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EPA+DHAは魚油に含まれるn-3系多価不飽和脂肪酸
他の名前:
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プラセボコンパレーター:プラセボ群
プラセボによる 12 週間の毎日の経口療法 (1 日合計 2.5 mL の鉱物油を摂取するための 3 つの不透明なソフトジェル)
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プラセボには鉱物油が含まれています
他の名前:
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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 |
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE5
時間枠:0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE5 measured in pg/mL at Weeks 4, 8 and 12. 5-HEPE (5-hydroxy-eicosapentaenoic acid) is an eicosanoid derived from eicosapentaenoic acid (EPA) via the 5-lipoxygenase pathway.
It functions as an anti-inflammatory lipid mediator, in part through the generation of reactive oxygen species.
Plasma levels of 5-HEPE (also known as HEPE5) were measured using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE11
時間枠:0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE11 measured in pg/mL at Weeks 4, 8 and 12. 11-HEPE (11-hydroxy-5Z,8Z,12E,14Z,17Z-eicosapentaenoic acid) is a monohydroxy fatty acid derived from eicosapentaenoic acid (EPA).
In research, it is commonly studied as a lipid mediator (eicosanoid) associated with anti-inflammatory processes.
Plasma levels of 11-HEPE (also known as HEPE11) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE12
時間枠:0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE12 at Weeks 4, 8 and 12. 12-HEPE (12-hydroxyeicosapentaenoic acid) is an omega-3 fatty acid metabolite formed from eicosapentaenoic acid (EPA) via the 12-lipoxygenase pathway.
It functions as a signaling lipid that helps mediate the beneficial effects of EPA and exhibits potent anti-inflammatory properties.
Plasma levels of 12-HEPE (HEPE12) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE15
時間枠:0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE15 measured in pg/mL at Weeks 4, 8 and 12. 15-HEPE (15-hydroxyeicosapentaenoic acid) is an anti-inflammatory metabolite produced from the omega-3 fatty acid eicosapentaenoic acid (EPA) via the 15-lipoxygenase pathway.
It functions as a pro-resolving lipid mediator, contributing to the resolution of inflammation.
Plasma levels of 15-HEPE (HEPE15) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Intervention Effects on Plasma Levels of Lipid Mediator of Inflammation HEPE18
時間枠:0, 4, 8 and 12 weeks
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Intervention effects on plasma levels of lipid mediator of inflammation HEPE18 measured in pg/mL at Weeks 4, 8 and 12. 18-HEPE (18-hydroxyeicosapentaenoic acid) is an anti-inflammatory metabolite of the omega-3 fatty acid eicosapentaenoic acid (EPA) and serves as a precursor for E-series resolvins.
E-series resolvins actively terminate inflammatory responses, promote the resolution of inflammation, and support tissue repair.
They exert potent anti-inflammatory effects by limiting neutrophil infiltration and suppressing pro-inflammatory cytokine production.
Plasma levels of 18-HEPE (HEPE18) were quantified using liquid chromatography-mass spectrometry.
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0, 4, 8 and 12 weeks
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Comparison of Intervention and Control Groups in IL-1β Levels (Log pg/mL)
時間枠:0, 4, 8 and 12 weeks
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Plasma levels of IL-1β were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma IL-1β levels expressed as log-transformed concentrations (pg/mL). The IL-1β data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in IL-1β levels. |
0, 4, 8 and 12 weeks
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Comparison of Intervention and Control Groups in IL-6 Levels (Log pg/mL)
時間枠:0, 4, 8 and 12 weeks
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Plasma levels of IL-6 were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma IL-6 levels expressed as log-transformed concentrations (pg/mL). The data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in IL-6 levels. |
0, 4, 8 and 12 weeks
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1. Comparison of Intervention and Control Groups in TNF-α Levels (Log pg/mL)
時間枠:0, 4, 8 and 12 weeks
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Plasma levels of TNF-α were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma TNF-α levels expressed as log-transformed concentrations (pg/mL). The data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in TNF-α levels. |
0, 4, 8 and 12 weeks
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Comparison of Intervention and Control Groups in IFN-γ Levels (Log pg/mL)
時間枠:0, 4, 8 and 12 weeks
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Plasma levels of IFN-γ were quantified using a commercially available V-PLEX Human Biomarker Plex Kit (Meso Scale Diagnostics). Reported values reflect the group plasma IFN-γ levels expressed as log-transformed concentrations (pg/mL). The data are presented on a logarithmic (log) scale to normalize the distribution of cytokine concentrations, which are typically right-skewed. Because log-transformed values are used, negative means can occur when the original (raw) cytokine concentrations are less than 1 (in the units of measurement, pg/mL). Thus, the negative values at baseline do not indicate 'negative' cytokine levels, but rather low concentrations on the original scale. Across time points, less negative (i.e., higher) log values indicate higher cytokine concentrations, whereas more negative values indicate lower concentrations. Therefore, changes in the mean log values over time reflect relative increases or decreases in IFN-γ levels. |
0, 4, 8 and 12 weeks
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) Activation (Log Cells/µL)
時間枠:0, 4, 8 and 12 weeks
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Reported values reflect PMN activation in plasma, expressed as log-transformed concentrations (cells/µL) at Weeks 4, 8, and 12.
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0, 4, 8 and 12 weeks
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) - Derived Matrix Metalloproteinase-8 (MMP-8) Levels (Log pg/mg) in Wound Fluid
時間枠:0, 4, 8 and 12 weeks
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MMP-8, also known as neutrophil collagenase, is an enzyme that degrades collagen types I, II, and III and contributes to tissue remodeling and inflammatory processes.
Wound fluid levels of MMP-8 were quantified using the MMP-8, neutrophil collagenase, Biotrak enzyme-linked immunosorbent assay kit (GE Healthcare Bio-Sciences Corp., Piscataway,NJ).
Reported values reflect wound fluid MMP-8 levels, expressed as log-transformed concentrations (pg/mg) at Weeks 0, 4, 8, and 12.
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0, 4, 8 and 12 weeks
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Intervention Effects on Polymorphonuclear Leukocyte (PMN) - Derived Human Neutrophil Elastase (HNE, ELA2) Levels (Log pg/mg) in Wound Fluid
時間枠:0, 4, 8 and 12 weeks
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HNE is a potent serine protease stored in neutrophil granules that plays a key role in degrading bacteria and host tissue during inflammatory responses.
Wound fluid levels of HNE were quantified using the InnuozymeTM Human Neutrophil Elastase Immunocapture Activity Assay Kit (Calbiochem, EMD Biosciences Inc., San Diego, CA).
Reported values reflect wound fluid HNE levels, expressed as log-transformed concentrations (pg/mg) at Weeks 0, 4, 8 and 12.
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0, 4, 8 and 12 weeks
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Comparison of Intervention vs. Control Groups in the Percent Change in Wound Area Relative to Baseline
時間枠:0, 4, 8 and 12 weeks
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Percentage Area Reduction (PAR) is a valuable, widely used metric for evaluating and comparing the effectiveness of wound healing interventions in research. PAR was calculated at each follow-up time point (Weeks 4, 8, and 12) relative to the baseline. It represents the percentage change in wound size (area in cm2) from baseline, computed as: "PAR"=("Baseline Area" -"Follow-up Area" )/"Baseline Area" ×100 Positive PAR values indicate a reduction in wound area (i.e., healing), whereas negative values indicate an increase in wound size compared to baseline (i.e., the wound has enlarged). |
0, 4, 8 and 12 weeks
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Venous Insufficiency Epidemiological and Economic Study Quality Of Life/Symptom (VEINES-QOL/Sym) Questionnaire
時間枠:0, 12 weeks
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The VEINES-QOL/Sym questionnaire consists of 26 items designed to assess both disease-specific quality of life (VEINES-QOL) and symptom severity (VEINES-Sym) in individuals with venous disorders.
The instrument evaluates two separate metrics, both of which are calculated using the mean of standardized z-scores.
The typical theoretical range for both is roughly 0 to 100, with a mean population standard of 50.
The final score was calculated after calculating the mean of all z scores, which were multiplied by 10, and then added to 50.
Higher scores indicate better quality of life and fewer symptoms (i.e., a more favorable outcome).
VEINES-QOL/Sym scores are expressed as Z-scores standardized to a reference population, with a mean of 0 and standard deviation of 1.
A Z-score of 0 represents the population mean.
Higher Z-scores indicate better quality of life and fewer venous insufficiency symptoms, while lower Z-scores indicate worse outcomes.
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0, 12 weeks
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Venous Clinical Severity Score (VCSS)
時間枠:0, 4, 8, 12 weeks
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The Venous Clinical Severity Score (VCSS) is a 10-item, 30-point scoring system used to assess and track the severity of chronic venous disease (CVD) and its response to treatment, ranging from 0 (none) to 3 (severe) for parameters like pain, ulcers, and edema.
Scores can range from 0 to 30 with higher scores meaning more severe venous disease.
The average scores at Weeks 0, 4, 8 and 12 were calculated for each treatment group.
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0, 4, 8, 12 weeks
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協力者と研究者
スポンサー
捜査官
- 主任研究者:Jodi C McDaniel, PhD、Ohio State University, College of Nursing
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 (実際)
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 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- 2018H0261
- R01AG059981 (米国 NIH グラント/契約)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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