Programmed Intermittent Bolus Dosing Versus Continuous Epidural Infusion for Epidural Analgesia in Abdominal Surgery.
A Prospective, Randomized Analysis of Epidural Anesthesia Using Programmed Intermittent Epidural Boluses Versus Continuous Epidural Infusion in Patients Undergoing Abdominal Surgery.
調査の概要
詳細な説明
研究の種類
入学 (実際)
段階
- フェーズ 4
連絡先と場所
研究場所
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California
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San Francisco、California、アメリカ、94158
- University of California San Francisco
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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:
- American Society of Anesthesia physical classification I - III, scheduled for surgery with anticipated an epidural anesthesia (including but not limited to colorectal, surgical oncology, urology, gynecology) as part of their perioperative treatment
Exclusion Criteria:
- Age younger than 18 years of age, non-English speaking, contraindication for neuraxial anesthesia (such as, but not limited to coagulopathy, infection at site, allergy to local anesthetic), preexisting neurologic deficits, inability to consent due to cognitive dysfunction, patients with pain numeric rating score > 5 each day for greater than 3 months, daily opioid consumption > 100 oral morphine equivalents for 14 consecutive days prior to surgery, patient refusal.
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 |
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アクティブコンパレータ：Continuous epidural infusion
At our institution, the most commonly utilized form of administration of medication through an epidural (our active comparator/control) is as follows: Combination of 0.0625% bupivacaine with 2mcg/ml of fentanyl infused at a constant rate of 8ml/hr. The patient has the ability to self administer patient controlled epidural analgesia of 2ml of the epidural medication with a lock out period of 15 min. The total maximum volume of epidural medication each hour is 16ml. These settings are managed and controlled by a epidural medication pump. Additional oral and intravenous analgesia medications are available as scheduled and pro re nata. |
他の名前：
他の名前：
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実験的：Programmed intermittent epidural bolus
For the programmed intermittent epidural bolus group: Combination of 0.0625% bupivacaine with 2mcg/ml of fentanyl will be administered as a bolus of 4ml every 30 minutes. The patient has the ability to self administer patient controlled epidural analgesia of 2ml of the epidural medication with a lock out period of 10 min. The total maximum volume of epidural medication each hour is 16ml. These settings are managed and controlled by a epidural medication pump. Additional oral and intravenous analgesia medications are available as scheduled and pro re nata. |
他の名前：
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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Total Local Anesthetic Utilized in First 24 Hours
時間枠：In first 24 hours
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Total local anesthetic consumed while epidural in place, recorded on infusion pump
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In first 24 hours
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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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Total Opioid Consumed
時間枠：While epidural in place (up to 72 hours post operatively)
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Total opioid consumed (intravenous or po) while epidural in place
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While epidural in place (up to 72 hours post operatively)
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Patient Satisfaction Score
時間枠：While epidural in place (up to 72 hours postoperatively)
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Ranked patient satisfaction scores while epidural in place. Measured by modified pain inventory. Minimum is 0, maximum of 10. 10 indicates highest patient satisfaction. |
While epidural in place (up to 72 hours postoperatively)
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Average Pain Severity
時間枠：While epidural in place (up to 72 hours postoperatively)
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Measured by modified pain inventory on a daily basis while epidural in place.
Minimum is 0, maximum is 10. 10 indicates highest pain severity.
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While epidural in place (up to 72 hours postoperatively)
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Incidence of Hypotension
時間枠：While epidural in place (24 hours postoperatively)
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Most common side effect post-operatively with epidural anesthesia.
Documented by recorded vitals signs, fluid resuscitation, and temporary cessation of epidural medication.
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While epidural in place (24 hours postoperatively)
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Worst Reported 24 Hour Pain
時間枠：While epidural in place (up to 72 hours postoperatively)
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Minimum is 0, maximum is 10. 10 indicates highest pain severity.
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While epidural in place (up to 72 hours postoperatively)
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Average Pain Interference
時間枠：While epidural in place (up to 72 hours postoperatively)
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Minimum is 0, maximum is 10. 10 indicates highest pain interference.
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While epidural in place (up to 72 hours postoperatively)
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協力者と研究者
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。
痛み、急性の臨床試験
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Bingol UniversityAtaturk Universityまだ募集していません術前不安 | 恐れ | PAİN
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Dexa Medica Group完了
フェンタニルの臨床試験
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University Hospitals Cleveland Medical Center募集