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临床试验/NCT02085694
NCT02085694Unknown2 期

A Pilot Study on the Efficacy of Lactobacillus Brevis CD2 Lozenges in Preventing Oral Mucositis by High-dose Chemotherapy With Autologous Hematopoietic Stem Cell Transplantation

Catholic University of the Sacred Heart1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2014年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
10
试验地点
1
主要终点
COMMON TERMINOLOGY CRITERIA FOR ADVERSE EVENTS v4.03 (CTCAE) for evaluation of change in oral mucositis

研究概览

简要总结

A pilot study on efficacy of Lactobacillus CD2 lozenges in preventing oral mucositis (OM) by high-dose chemotherapy with autologous hematopoietic stem cell transplantation. To test whether the probiotic Lactobacillus brevis CD2 lozenges can reduce the incidence and severity of high-dose chemotherapy conditioning regimen induced OM in patients undergoing HSCT.

Clinical activity will be defined as reduction in the incidence of chemotherapy induced OM in the patients undergoing HSCT.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 65 years
  • Karnofsky Performance Score ≥ 70%.
  • Confirmed histological diagnosis of multiple myeloma for which HSCT is as approved modality of therapy
  • Patients eligible to receive high-dose chemotherapy as part of conditioning regimen
  • Concomitant co morbid condition if present, controlled by ongoing treatments (e.g. hypertension, diabetes and so on)
  • Serum creatinine < 1.8mg/dl
  • Total bilirubin < 2mg/dl
  • Liver enzymes within three times of normal limit
  • Expected survival > 6 months.

排除标准

  • Pregnant women and lactating mothers
  • Patients with history of HIV infection
  • Patients who have taken any other investigational product in last 4 weeks
  • Patients having untreated symptomatic dental infection
  • Patients with WHO Grade 3 or 4 oral Mucositis
  • Other serious concurrent illness
  • Inconclusive hematological diagnosis
  • Patients with signs and symptoms of systemic infections
  • Patient's/guardian's refusal to sign informed consent

研究组 & 干预措施

Lactobacillus brevis CD2 lozenges

Experimental

干预措施: Lactobacillus brevis CD2 (Drug)

结局指标

主要结局

COMMON TERMINOLOGY CRITERIA FOR ADVERSE EVENTS v4.03 (CTCAE) for evaluation of change in oral mucositis

时间窗: days -14;-7; 0;+7;+14;+21

次要结局

  • COMMON TERMINOLOGY CRITERIA FOR ADVERSE EVENTS v4.03 (CTCAE) to determine the incidence of Grade I and II OM(days -14;-7; 0; +7;+14; +21)

研究者

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

sabrina giammarco

MD

Catholic University of the Sacred Heart

研究点 (1)

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