跳至主要内容
临床试验/NCT00851448
NCT00851448终止不适用

Safety, Tolerance and Efficacy of an Oral Nutritional Supplement in Lung Cancer Patients. A Randomised, Double-blind, Controlled Pilot Study

Fresenius Kabi3 个研究点 分布在 2 个国家目标入组 17 人开始时间: 2009年10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
终止
入组人数
17
试验地点
3
主要终点
compliance to nutrition therapy

研究概览

简要总结

To test the compliance, tolerance, safety and to get preliminary insights into the efficacy of a new oral nutritional supplement (containing n-3 fatty acids, amino acids and antioxidants) designed to prevent or delay cachexia and anorexia in lung cancer patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Investigator)

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
否

入选标准

  • •non-small cell lung cancer patients stage IIIb or IV
  • •planned chemotherapy or combined chemo-/radiotherapy
  • •current body weight less than 6 months ago
  • •abnormal CRF level
  • •BMI >=20 kg/m2 and <=30kg/m2

排除标准

  • •significant oedema in the time of screening and randomisation
  • •concomitant inflammatory diseases
  • •active infections including HIV and AIDS
  • •liver failure
  • •chronic renal failure or cardiac pacemaker
  • •chronic heart failure
  • •insulin treated diabetes mellitus
  • •medications that impair sex hormone synthesis, secretion or function
  • •acute or chronic infections
  • •body weight loss > 5% during the last 6 months or > 10% during the last 10 months
  • •fish oil supplementation within 3 months prior to study entry
  • •taking vitamins in doses greater than recommended daily allowance
  • •life expectancy less than 6 months in the opinion of the investigator

研究组 & 干预措施

1

Experimental

Oral nutritional supplement containing n-3 fatty acids, amino acids, antioxidants

干预措施: oral nutritional supplement, food for special medical purposes (Dietary Supplement)

2

Placebo Comparator

isocaloric, isonitrogenous

干预措施: oral nutritional supplement, food for special medical purposes (Dietary Supplement)

结局指标

主要结局

compliance to nutrition therapy

时间窗: baseline, months 1, 2, 3, 4

次要结局

  • ECOG performance status(baseline, months 1, 2, 3, 4)
  • anorexia questionnaire(baseline, months 1, 2, 3, 4)
  • gastrointestinal syndrome score (GIS)(baseline, months 1, 2, 3, 4)
  • body cell mass(baseline, months 1, 2, 3, 4)
  • weight change(baseline, months 1, 2, 3, 4)
  • hand grip strength(baseline, months 1, 2, 3, 4)

研究者

申办方类型
Industry

研究点 (3)

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