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临床试验/NCT00831064
NCT00831064已完成不适用

A Randomized Controlled Trial of Four Different Bowel Cleansing Regimens Prior to Colonoscopy: Efficacy, Patient Tolerability and Safety

University of Alberta1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2007年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
200
试验地点
1
主要终点
bowel preparation quality as measured by the Ottawa scale

研究概览

简要总结

To compare 4 commonly used bowel preparations in terms of efficacy, patient tolerability and safety. All these 4 bowel preparations are likely to be efficacious and safe. However, those with lower volume are likely to be better tolerated and completed by patients.

详细描述

Adequate bowel preparation is imperative for diagnostic accuracy and therapeutic safety. Several bowel cleansing preparations have been approved by Health Canada and are commonly used prior to colonoscopy. Polyethylene glycol (PEG) has been considered to be the "gold standard" for bowel preparation. It is a nonabsorbable solution which passes through the bowel without net absorption or secretion. Significant fluid and electrolyte shifts are therefore avoided. However, the large volume (4 liters), the salty taste and the sulphur smell frequently lead to poor tolerability and compliance, sometimes resulting in inadequate bowel preparation. Several other bowel cleansing preparations have been developed and include sodium phosphate (NaP), magnesium citrate, and sodium picosulphate plus magnesium oxide (PSMC)-containing preparations. NaP is a low volume hyperosmotic solution which draws plasma water into the bowel lumen to promote colonic cleansing. As a result, significant fluid and electrolyte shifts can occur. The advantage of the low volume is better patient tolerance compared to PEG. However, even in healthy individuals severe electrolyte disturbances have been reported when the 2 required doses are taken 12 hours apart. Therefore Health Canada has recommended that 2 doses of NaP be taken 24 hours apart. Patients with renal failure, congestive heart failure and liver failure should avoid this preparation (Grade I A). PSMC is a hyperosmotic saline laxative which increases intraluminal volume resulting in increased intestinal motility. Magnesium, a constituent of PSMC, stimulates the release of cholecystokinin which also stimulates intestinal motility. Since magnesium is eliminated by the kidney, patients with renal insufficiency or failure should also avoid this preparation.

Many randomized controlled trials have compared the efficacy and tolerability of various bowel cleansing regimens. Studies comparing full-volume (4 liters) PEG with low-volume (2 liters) PEG combined with magnesium citrate or bisacodyl have demonstrated equal efficacy of colonic cleansing but with improved patient tolerance. However, there is little data on how low volume PEG compares with NaP. The only meta-analysis of twenty nine trials on optimal bowel preparation concluded that NaP was more effective in bowel cleansing than 4-liter PEG or PSMC. However, there were only three trials comparing NaP to PSMC that met inclusion and exclusion criteria in this meta-analysis and the results have been conflicting. Also there were only three trials comparing PEG to PSMC in this meta-analysis with inconclusive data. Moreover, the mean number of patients per trial was small at 223, with the highest number of patients in a trial at 500.

A consensus document prepared by three leading American gastrointestinal societies (American Society of Gastrointestinal Endoscopy, American Society of Colon and Rectal Surgeons and Society of American Gastrointestinal and Endoscopic Surgeons) as well as a position paper by the Canadian Association of Gastroenterology identified the lack of an ideal bowel preparation which meets all these criteria. Furthermore, the need for further studies was identified in the following areas:

  1. Two-liter PEG vs NaP
  2. PSMC vs NaP

Outpatients who need to undergo routine colonoscopy will be recruited. Each patient will be randomly assigned to one of the four bowel preparations after they have given consent to participate in the study:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Male or female between the ages of 18 and
  • •Planned elective outpatient colonoscopy.

排除标准

  • •History of renal insufficiency or abnormal creatinine clearance with GFR <
  • •History of congestive heart failure.
  • •History of acute coronary syndrome or unstable angina.
  • •History of liver cirrhosis or ascites.
  • •Chronic lasix therapy.
  • •History of colorectal resection.
  • •Known or suspected bowel obstruction, megacolon or ileus

研究组 & 干预措施

3. NaP

Active Comparator

90 cc NaP PO

干预措施: colonoscopy bowel prep (Procedure)

2. 2L PEG plus bisacodyl

Active Comparator

2L PEG PO + 4 tablets bisacodyl PO

干预措施: colonoscopy bowel prep (Procedure)

1. 4L PEG only

Active Comparator

4L PEG PO

干预措施: colonoscopy bowel prep (Procedure)

4. PSMC plus Mg-citrate

Active Comparator

PSMC plus 300 cc Mg-citrate PO

干预措施: colonoscopy bowel prep (Procedure)

结局指标

主要结局

bowel preparation quality as measured by the Ottawa scale

时间窗: at the time of endoscopy

次要结局

  • patient tolerability of bowel preparation(at the time of colonoscopy)
  • electrolyte and renal function abnormalities(2 sets of measurements will be obtained: prior to the start of bowel preparation and at the time of colonoscopy)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dina Kao

Associate Professor

University of Alberta

研究点 (1)

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