跳至主要内容
临床试验/NCT00900068
NCT00900068终止不适用

Substance P Follow-up to a Pilot Study of Aprepitant vs Placebo Combined With Standard Antiemetics for the Control of Nausea and Vomiting During Hematopoietic Cell Transplantation

OHSU Knight Cancer Institute1 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2008年8月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
9
试验地点
1
主要终点
Average, median, and mode for substance P levels at different times

研究概览

简要总结

RATIONALE: Studying samples of blood in the laboratory from patients with cancer may help doctors learn more about nausea and vomiting caused by cancer treatment.

PURPOSE: This laboratory study is looking at blood samples from patients with cancer who were treated on a clinical trial to control nausea and vomiting during donor stem cell transplant.

详细描述

OBJECTIVES:

Primary

  • To compare the amount of substance P in serum samples from patients with cancer treated with busulfan/cyclophosphamide or cyclophosphamide/total body irradiation conditioning regimens prior to undergoing allogeneic hematopoietic stem cell transplantation.

Secondary

  • To assess the changes in substance P over time to see if there is an optimal time shown by this physiologic correlate to discontinue substance P blockade after the chemotherapy regimen is completed in these patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Average, median, and mode for substance P levels at different times

次要结局

  • Correlation of substance P levels with patient response (emesis or not)

研究者

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

Joseph Bubalo

PharmD

OHSU Knight Cancer Institute

研究点 (1)

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