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临床试验/NCT02763033
NCT02763033已完成2 期

Dietary Manipulation of the Microbiome-metabolomic Axis for Mitigating GVHD in Allo HCT Patients

University of Michigan Rogel Cancer Center1 个研究点 分布在 1 个国家目标入组 107 人开始时间: 2017年4月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
107
试验地点
1
主要终点
Incidence of grade II-IV GVHD

研究概览

简要总结

Investigators are evaluating the feasibility, safety and early efficacy of administering a commercially available dietary supplement containing potato-based resistant starch to subjects undergoing allogeneic SCT (stem cell transplant). The intervention will begin immediately prior to the conditioning phase and continue through day 100. Investigators hypothesize that short term administration of a resistant starch is capable of increasing levels of butyrate within the intestine that will reduce rates of acute GVHD (Graft-Versus-Host Disease).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

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

入选标准

  • Subjects undergoing matched related and matched unrelated full intensity allogeneic HSCT.
  • Age ≥ 18 years for the feasibility phase. Age ≥10 years old AND ≥50 kg for the phase II portion.
  • Karnofsky >70%, (Karnofsky Performance Status: an attempt to quantify cancer patients' general well-being and activities of daily life. The score ranges from 0 to 100 where 100 is "perfect" health and 0 is death.)
  • Subjects must be able to swallow capsules/tablets
  • Ability to understand and the willingness to sign a written informed consent
  • Willingness to consent / co-enroll on BMT long term follow up study or HUM00043287 (UMCC2001-0234)
  • Availability of an HLA matched related or matched unrelated donor

排除标准

  • Patients with inflammatory bowel disease.
  • Patients with a history of gastric bypass surgery.
  • Patients with active Clostridium difficile infection at the time of study enrollment. Active infection is defined as a stool sample positive for Clostridium difficile toxin via EIA (enzyme immunoassay) and either symptoms (frequent loose stools) OR imaging findings consistent with toxic megacolon.
  • Patients actively enrolled on any other GVHD prevention trial.
  • Any physical or psychological condition that, in the opinion of the investigator, would post unacceptable risk to the patient or raise concern that the patient would not comply with protocol procedures.

研究组 & 干预措施

Bob's Red Mill®

Experimental

Patients will follow the standard BMT (bone marrow transplant) diet and add potato-starch produced by Bob's Red Mill® beginning on day -7 and continuing through day +100.Patients will consume 20 g of Bob's Red Mill®, Potato-based dietary starch, orally twice daily.

Initially, subjects will take 20g daily for first three days prior to increasing dose to 20 g BID.

干预措施: Bob's Red Mill® (Drug)

Bob's Red Mill®

Experimental

Patients will follow the standard BMT (bone marrow transplant) diet and add potato-starch produced by Bob's Red Mill® beginning on day -7 and continuing through day +100.Patients will consume 20 g of Bob's Red Mill®, Potato-based dietary starch, orally twice daily.

Initially, subjects will take 20g daily for first three days prior to increasing dose to 20 g BID.

干预措施: Starch Placebo (Other)

Starch Placebo

Placebo Comparator

Patients will receive an iso-caloric, non-resistant starch placebo.

干预措施: Starch Placebo (Other)

结局指标

主要结局

Incidence of grade II-IV GVHD

时间窗: Day 100

The incidence of grade II, III and IV GVHD (Graft Versus Host Disease) as documented on day 100 Grade II: Rash 25-50% of Body Surface Area (BSA), Bilirubin 3.1-6mg/dL, adult stool output 1000-1500mL/day or child 20-30mL/kg/day. Grade III: Rash greater than 50% BSA, bilirubin 6.1-15mg/dL, adult stool output greater than 1500mL/day or child stool output greater than 30mL/kg/day Grade IV: generalized erythroderma plus bullous formation and desquamation greater than 5% BSA, bilirubin greater than 15mg/dL, severe abdominal pain with or without ileus, or grossly bloody stool.

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 (1)

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