Effects of Dexmedetomidine During Radiofrequency Ablation of Abdominal Tumours
Effects of Dexmedetomidine on Periprocedural Pain During Radiofrequency Ablation of Liver and Kidney Tumours
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
Although radiofrequency ablation (RF) is accepted as the best therapeutic choice for patients with early stage hepatocellular carcinoma when liver transplantation or surgical resection are not suitable options, it is still performed only in a few hospitals and experience is so far limited (Goldberg & Ahmed, 2002; Shiina et al., 2005). In addition, RF ablation is emerging as a viable alternative to surgery for inoperable patients with limited hepatic metastatic disease, especially from colorectal cancer. Although radiofrequency ablation has been accepted as a safe and effective treatment for liver and kidney tumours, there are few studies addressing periprocedural pain.
Thus, the optimal anaesthetic procedure is still to be determined. Currently at our institution RF is performed as monitored sedation procedure using remifentanil infusion supplemented with midazolam boluses, when considered necessary. However, when using remifentanil and midazolam combination it is quite difficult to avoid too deep respiratory depression.
Dexmedetomidine is an α2-adrenoreceptor agonist with sedative, analgesic and anxiolytic effects, and it has more selective α2-adrenergic effect than clonidine. Dexmedetomidine has a great deal of potential in this arena given its analgesic and anxiolytic properties while preserving respiratory drive (Bergese SD et al., 2010).
All patients will receive dexmedetomidine 0.4 µg/kg/hr infusion from the start of procedure. The infusion will be continued during the whole RF procedure.
At the same time all patients will receive remifentanil infusion according to TCI (target controlled infusion) protocol. Plasma concentration target will be set from 0.5 ng/ml and, if necessary, will be increased to achieve a comfortable state of patient (Ramsey Sedation Scale: 2-3).
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- フェーズ 4
連絡先と場所
研究場所
-
-
-
Uppsala、スウェーデン、75185
- Uppsala University Hospital
-
-
参加基準
適格基準
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:
- liver or/and kidney cancer for which radiofrequency ablation procedure is planned
- signed informed consent form
Exclusion Criteria:
- patient refusal
- pregnancy
- known allergy to dexmedetomidine or remifentanil
- atrioventricular block grade II or III or other significant cardiac conduction disturbance
- stroke
- low blood pressure not responding to treatment
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:なし
- 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)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:デクスメデトミジン
|
Dexmedetomidine 0.4 µg/kg/hr infusion during RF procedure
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Patient Satisfaction With Sedation Technique
時間枠:After completion of procedure (within 15 minutes)
|
Rating of how satisfied the patient was with their sedation on a scale of 1-5 with 1 being very dissatisfied and 5 being extremely satisfied
|
After completion of procedure (within 15 minutes)
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Vital signs: blood pressure, oxygen saturation, heart rate, breathing rate
時間枠:During procedure and up to 2 hours stay at the post-anesthesia care unit
|
During procedure and up to 2 hours stay at the post-anesthesia care unit
|
|
|
Ramsey Sedation Scale Score
時間枠:During the procedure and up to 2 hours stay at the post-anesthesia care unit
|
Rating of depth of sedation.
Scale 1 - 6, 1 being wide awake and 6 being non-responsive
|
During the procedure and up to 2 hours stay at the post-anesthesia care unit
|
|
Maximal pain intensity
時間枠:During procedure and up to 2 hours stay at the post-anesthesia care unit
|
The 11-point Numerical Rating Scale (NRS) to assess periprocedural pain.
Scale of 0-10, with 0:no pain and 10: pain as bad as it could be
|
During procedure and up to 2 hours stay at the post-anesthesia care unit
|
協力者と研究者
捜査官
捜査官
- 主任研究者:Egidijus Semenas, MD, PhD、Uppsala University Hospital, Uppsala, Sweden
- 主任研究者:Mats Eriksson, MD, PhD、Uppsala University Hospital, Uppsala, Sweden
研究記録日
主要日程の研究
研究開始
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
最初の投稿
学習記録の更新
投稿された最後の更新 (見積もり)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- RF-01
- 2013/409 (Uppsala Regional Ethics Committee)
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