Preventing Acute Kidney Injury and Improving Outcome in Critically Ill Patients Utilising Risk Prediction Score (PRAIOC-RISKS)
Preventing Acute Kidney Injury and Improving Outcome in Critically Ill Patients Utilising Risk Prediction Score - a Pilot Feasibility Randomized Controlled Trial
調査の概要
詳細な説明
Background and rationale AKI is common in the intensive care unit .It contributes significantly to mortality and morbidity .the estimated incidence or AKI among critically ill patients is 30-40% and morality is high.
There is a well recognized gap between the optimal care and the delivered care regarding prevention and management of AKI.
The focus over the last few years has been on early detection. A panel of urinary biomarkers have proved helpful for early detection of AKI. However the cost and low specificity make no single one of them solely reliable .using a panel of bio-markers increases their specificity.
The concept of electronic alerts has been recently introduced. Some trials have been testing its impact on the outcome of AKI. The benefit of electronic alerts is still uncertain .A meta-analysis is currently underway to synthesize stronger evidence of electronic alerts benefit.
Another evolving area, is the development of risk score to predict AKI and and hence applying timely preventive measures.
KDIGO recommends applying preventive measures to high risk patients. However no study to date has tested risk scores based interventions
Hypothesis:
We will use the recently validated score to predict AKI in ICU patients. We will then apply preventive measures. To patients at risk .To our knowledge this is the first study to apply preventive interventions based on AKI risk score assessment
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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Cairo、エジプト
- Cairo University Hospitals
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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
受講資格のある性別
説明
Inclusion Criteria:
All adult patients (≥18 year old) admitted to the intensive care unit and do not fulfill the criteria for the diagnosis of AKI by Kidney Disease Improving Global Outcome (KDIGO) definition
Exclusion Criteria:
- Patients who have already developed AKI at the time of intensive care unit ICU admission.
- Patients with insufficient medical records to obtain previous medical history
- Patients who lack mental capacity
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：防止
- 割り当て：ランダム化
- 介入モデル：並列代入
- 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 |
|---|---|
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介入なし：Observational
patients will be recruited to this arm to observe prospectively the incidence of AKI among critically ill patients.patients
will receive the standard care.No other intervention will be delivered
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アクティブコンパレータ：Interventional
Patients in this arm will be subject to AKI risk score.
This risk score was recently developed and validated in Mayo clinic the intervention will be Measures to prevent AKI among critically ill patients
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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 |
|---|---|---|
|
Incidence of AKI
時間枠：during 7 days of ICU admission
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We will compare the incidence rate between the interventional and the observational arm
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during 7 days of ICU admission
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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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30 day mortality
時間枠：30 days
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all cause mortality during 30 days of ICU admission or within 30 days of developement of AKI
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30 days
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Time to recovery after development of AKI
時間枠：30 days
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Time interval between the diagnosis of AKI and recovery of either blood chemistry or oliguria
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30 days
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Deterioration of AKI stage
時間枠：30 days
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Transition from initial stage KDIGO stage 1 to either 2 or 3 .Transition from initial stage 2 to 3
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30 days
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Duration of dialysis dependency
時間枠：30 days
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time patient remains dialysis-dependant after severe AKI.
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30 days
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協力者と研究者
スポンサー
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
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。