ISRCTN72500766已完成不适用
Multicentre randomised controlled trial to compare stapled side-to-side anastomosis with sutured end-to-end anastomosis following resection for primary or recurrent Crohn's disease
Mount Sinai Hospital (Toronto) (Canada)0 个研究点目标入组 200 人开始时间: 2005年9月9日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Women and men aged greater than 16 years
- •2. Elective ileocolonic resection
- •3. Colonoscopy and Small Bowel Endoscopy (SBE) completed with the last 3 years
- •4. Crohn?s Disease involving the terminal ileum plus or minus right colonic disease
- •5. No other sites of involvement with Crohn?s disease in the Gastrointestinal (GI) tract current or past
- •6. Willing to return for colonoscopy at 12 months
排除标准
- •1. Require emergency surgery
- •2. Have sites of Crohn?s involvement elsewhere, except for minimal perianal disease
- •3. Have had strictureplasties or other resections for Crohn?s disease performed either at this operation or previously, the exception being resections for fistula disease in bowel not affected by Crohn?s disease
- •4. Require a bypass procedure or defunctioning ileostomy during the index procedure
- •5. Have compromised renal function (serum creatinine level greater than 130 mmol/l or 1.5 mg/l)
- •6. Prednisone, budesonide, 5-Aminosalicylic Acid (5-ASA) medications, ciprofloxacin, metronidazole, cyclosporin and Anti-Tumour Necrotising Factor (Anti-TNF) and any other medications used to treat Crohn?s cannot be discontinued postoperatively
- •7. Are unable or willing to give informed consent and return for a colonoscopy at 12 months
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