Interscalene and Combined Supra Scapular and Axillary Nerve Blocks in Rotator Cuff Repair
A Randomized Comparison of Inter Scalene and Combined Supra Scapular and Axillary Nerve Blocks for Postoperative Pain Relief in Arthroscopic Shoulder Rotator Cuff Repair
調査の概要
詳細な説明
Patients having elective arthroscopic rotator cuff repair will be randomized to one of the two groups.
Group 1: This group will receive Interscalene block (ultrasound guided and nerve stimulator aided) followed by a general anesthesia.
Group 2: This group will receive Suprascapular and Axillary nerve block (ultrasound guided and nerve stimulator aided) followed by a general anesthesia.
Performance time, quality and efficacy as well as any side-effects of the blocks will be evaluated in terms of pain scores in recovery room, after 4- 6 hours and the next morning, opioid usage and patient satisfaction.
Primary hypothesis:
• Combined Suprascapular and axillary nerve blocks provide similar postoperative analgesia as compared to interscalene block for arthroscopic rotator cuff repair.
Secondary hypothesis
• Interscalene block is associated with more side effects and complications as compared to suprascapular nerve block and axillary nerve block.
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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Ontario
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London、Ontario、カナダ、N6A 4V5
- St. Joseph's Health Care
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London、Ontario、カナダ
- St. Joseph 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
説明
Inclusion Criteria:
- Elective shoulder arthroscopic rotator cuff repair
- ASA I - III (American Society of Anaesthesia Classification)
Exclusion Criteria:
- ASA IV or higher ( American Society of Anaesthesia Classification)
- Obesity: BMI >35
- Narcotic Abuse/ Drug dependency
- Major Neurologic deficits
- Allergy to local anesthetics
- Infection in the site of the puncture
- Mental impairment
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：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ：Interscalene block
This arm patients will receive inter scalene block which will be ultrasound and nerve stimulator guided.
|
This arm patients will receive inter scalene block which will be ultrasound and nerve stimulator guided.
|
|
アクティブコンパレータ：Suprascapular and Axillary nerve block
This arm patients will receive Suprascapular and axillary nerve blocks which will be ultrasound guided and nerve stimulator guided.
|
This arm patients will receive Suprascapular and axillary nerve blocks which will be ultrasound guided and nerve stimulator guided.
|
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 |
|---|---|---|
|
Analgesic Efficacy
時間枠：one year
|
Visual Analogue scores for pain will be analyzed using chi-squared test.
Interscalene block (ISB) of the brachial plexus has been demonstrated to be one of the most effective analgesic modality during arthroscopic shoulder surgery.
However, despite its (ISB) time-tested record of relative safety, ISB is associated with some complications.
These could be central nervous system, respiratory and cardiovascular complications.
These side effects and complications are based upon the anatomy of the brachial plexus at this level.Recently, suprascapular and axillary nerve blocks have been used to control postoperative shoulder pain.
The study will try to find out whether combined supra scapular and axillary nerve blocks are as effective in pain control as compared to inter scalene block.
|
one year
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Side effects
時間枠：1 year
|
The study will try to find out whether combined supra scapular and axillary nerve blocks are associated with less side effects as compared to inter scalene block.
|
1 year
|
その他の成果指標
結果測定 |
時間枠 |
|---|---|
|
Patient satisfaction
時間枠：1 year
|
1 year
|
協力者と研究者
捜査官
- 主任研究者：Shalini Dhir, MD, FRCPC、Western University, Canada
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 (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
その他の研究ID番号
- 102994
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
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。
interscalene blockの臨床試験
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Cairo Universityわからない
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Lawson Health Research Institute募集