Protocol for CAMUS Delphi Study
Protocol for CAMUS Delphi Study: A Consensus on Reporting of Complications After Urological Surgeries
調査の概要
詳細な説明
The CAMUS Delphi Study: A Consensus on Reporting of Complications After Urological Surgeries is a multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology. The initial survey consists of a 12-part questionnaire that will aim to reach consensus on a wide range of contentious issues in Urological surgery using the frameworks of both the established Clavien-Dindo Classification (CDC) and the new CAMUS Classification.
To ensure comprehensive and comparable complication reporting across centres worldwide, a conclusive uniform language for reporting complications must be created and subsequently integrated. Accurate reporting will allow for more precise allocation of resources, improve unit efficiency, and reduce healthcare burden, while providing clinicians with a better understanding of intra- and post-operative morbidity. If a comprehensive, homogenous reporting construct is integrated worldwide, the potential to build and develop a universal database with complications from all centres around the world will surely provide invaluable data to create new guidelines and recommendations, ultimately improving patient counselling and surgical quality of care.
研究の種類
入学 (予想される)
連絡先と場所
研究場所
-
-
-
Melbourne、オーストラリア
- The Royal Melbourne Hospital
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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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Local and international consultant Urologists, accredited Urology trainees, consultant Anaesthetists and consultant ICU specialists will be invited to complete the survey. Critical care physicians who are primarily Urological anaesthetists or have experience in complication reporting will be targeted.
Exclusion Criteria:
- All other specialists that do not meet the inclusion criteria.
- Under 18 years of age.
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
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
Urologists
Local and international consultant Urologists and accredited Urology trainees.
|
Multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology.
|
|
Anaesthetists
Local and international consultant anaesthetists.
Critical care physicians who are primarily Urological anaesthetists or have experience in complication reporting will be targeted.
|
Multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology.
|
|
ICU specialists
Local and international consultant ICU specialists.
Critical care physicians who are primarily Urological focused or have experience in complication reporting will be targeted.
|
Multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology.
|
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 |
|---|---|---|
|
Standardised complication reporting in Urology
時間枠:6 months
|
Establish criteria for standardised complication reporting in Urology
|
6 months
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Marc A Furrer, MD、Melbourne Health
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 (予想される)
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
その他の研究ID番号
- 2020.046
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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