ISRCTN17667918已完成2 期
Feasibility study for a randomised controlled trial of bupivacaine, lignocaine with adrenaline, or placebo wound infiltration to reduce postoperative pain after laparoscopic cholecystectomy in West Africa
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 69
研究概览
简要总结
2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/31388637 (added 04/04/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Aged 18 years or older
- •2. Undergoing elective laparoscopic cholecystectomy for symptomatic gallstone disease
排除标准
- •1. American Society of Anesthesiology (ASA) physical status class 3+
- •2. Pregnant women
- •3. Acute cholecystitis
- •4. History of allergy to bupivacaine, lignocaine or related local anaesthetic drugs
- •4. Known peptic ulcer disease
- •5. Known opiate addiction
- •6. Known contraindications to use of NSAIDs such as bronchial asthma
- •7. If an abdominal drain is inserted or the operation was converted to an open procedure, the patient will not receive the allocated intervention and pain scores will not be collected
研究者
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