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[大阪地区结直肠癌预防的干预试验]

[Interventional trial for colorectal cancer prevention in Osaka].

作者信息

Ishikawa H

机构信息

Dept. of Cancer Epidemiology, Osaka Medical Center for Cancer and Cardiovascular Diseases.

出版信息

Gan To Kagaku Ryoho. 2000 Jul;27(8):1185-90.

Abstract

We established a protocol for an interventional randomized controlled trial for the prevention of colorectal tumors, in which special importance was attached to practicality. The subjects are patients with multiple colorectal tumors, who form a high risk group for colorectal cancer. Two regimens were formulated for the prevention of colorectal cancer. One was dietary guidance alone (Regimen I), and the other was dietary guidance plus the ingestion of wheat bran biscuits (Regimen II). One of the two regimens is assigned at random each week in advance, and the patients are recruited to receive the regimen of the week in which they are first examined, after giving informed consent. The dietary guidance aims to restrict the energy intake of oil and fat to 18-22% of the total energy intake. Biscuits with a wheat bran content of 30% by weight, which we developed, were prescribed at 25 g/day (7.5 g/day as wheat bran). The main end points of the trial were examinations for recurrence of colorectal tumors after 4 years. The target number of patients is 200 in total, i.e., 100 for each group. The recruiting of subjects was started in June, 1993, and finished in September, 1997; 100 (90%) of 115 patients recruited for Regimen I and 100 (88%) of 116 patients recruited for Regimen II consented to participate in the trial. No severe adverse effects have been reported, and the trial is progressing well. The trial will be completed in September, 2001, when the 4-year follow-up of the last patient will end.

摘要

我们制定了一项预防结直肠肿瘤的介入性随机对照试验方案,该方案特别注重实用性。研究对象为患有多发性结直肠肿瘤的患者,他们构成了结直肠癌的高危人群。制定了两种预防结直肠癌的方案。一种是单纯饮食指导(方案I),另一种是饮食指导加食用麦麸饼干(方案II)。每周提前随机分配两种方案中的一种,患者在签署知情同意书后,被招募接受首次检查所在周的方案。饮食指导旨在将油脂能量摄入限制在总能量摄入的18 - 22%。我们研发的麦麸含量为30%(重量)的饼干,规定每日食用25克(相当于每日食用7.5克麦麸)。该试验的主要终点是4年后结直肠肿瘤复发情况的检查。患者目标总数为200人,即每组100人。受试者招募于1993年6月开始,1997年9月结束;方案I招募的115名患者中有100名(90%)、方案II招募的116名患者中有100名(88%)同意参与试验。未报告严重不良反应,试验进展顺利。该试验将于2001年9月完成,届时最后一名患者的4年随访将结束。

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