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临床试验/NCT03108911
NCT03108911终止2 期

Gluten Free Diet for AML Patients Undergoing Induction Chemotherapy

Rutgers, The State University of New Jersey2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2017年7月27日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
1
试验地点
2
主要终点
Rate of compliance with GFD assessed using daily food intake diary

研究概览

简要总结

This randomized phase II trial studies how well a gluten free diet works in diminishing side effects in patients with acute myeloid leukemia undergoing induction chemotherapy. A gluten free diet may result in less intestinal side effects and blood infections during the induction chemotherapy compared to a standard diet.

详细描述

PRIMARY OBJECTIVES:

I. To determine if a gluten free diet (GFD) modulates the rate and severity of bacteremia and gastrointestinal toxicity (measured by total parenteral nutrition [TPN] or nothing by mouth [NPO] order) in patients undergoing standard acute myeloid leukemia (AML) induction chemotherapy.

SECONDARY OBJECTIVES:

I. To determine the tolerance of, and compliance with, a GFD in patients undergoing standard AML induction chemotherapy.

OUTLINE: Patients are randomized to 1 of 2 groups.

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
None

入排标准

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

入选标准

  • Patients undergoing AML induction chemotherapy with an anthracycline + cytarabine-based chemotherapy regimen
  • No history of celiac disease or non-celiac gluten sensitivity
  • No grade 3 or 4 gastrointestinal (GI) toxicity at time of initial screening
  • No documented bacteremia at time of initial screening
  • Eastern Cooperative Oncology Group (ECOG) performance status 0, 1 or 2 at time of initial screening

排除标准

  • Pregnant women

结局指标

主要结局

Rate of compliance with GFD assessed using daily food intake diary

时间窗: Up to 30 days

Adherence to diet will be recorded in a food diary. Compliance will be defined as \> 67% of meals being gluten free.

Rate and severity of bacteremia with enteric organisms during AML induction therapy assessed using stool samples

时间窗: Up to 30 days

To determine how often patients develop bacteremia during AML induction therapy

Rate and severity of GI symptoms during AML induction therapy

时间窗: Up to 30 days

To determine what the severity is if GI symptoms develops

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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