跳至主要内容
临床试验/NCT02087657
NCT02087657Unknown不适用

Pilot Study Exploring the Use of Hyperbaric Oxygen in Autologous Peripheral Blood Stem Cell Transplant

University of Kansas Medical Center2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年3月最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
2
主要终点
Presence or absence of a treatment limiting toxicity

研究概览

简要总结

By doing this study, researchers hope to learn the following:

  • The safety of hyperbaric oxygen administration in the setting of the autologous transplant
  • The effects of hyperbaric oxygen administration on neutrophil count recovery and engraftment

详细描述

The post stem cell transplant complications of neutropenic fever and mucositis, related to the chemotherapy and/or radiation on hematopoietic tissue administered prior to peripheral blood stem cell transplant, are reversible upon neutrophil count recovery. The investigators will investigate the use of hyperbaric oxygen as an intervention to shorten neutropenia post-high-dose chemotherapy and autologous peripheral blood stem cell transplant. The idea of using hyperbaric oxygen therapy in autologous stem cell transplantation is based on the investigators pre-clinical work that supported the use of hyperbaric oxygen to improve umbilical cord blood (cluster of differentiation 34) CD34+ stem cell transplantation.

研究设计

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

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Voluntary written informed consent
  • Subjects with Multiple Myeloma (MM), Hodgkin's Disease (HD), and non-Hodgkins lymphoma (NHL) who are eligible for high-dose chemotherapy and autologous PBSC transplant. Subjects should be enrolled within 30 days of transplant.
  • Subjects must be >/= 18 yrs old and </= 70 yrs old
  • Karnofsky performance status of >/= 70%
  • Adequate hepatic, renal, cardiac and pulmonary function to be eligible for transplant. Minimum criteria include:
  • ALT (alanine aminotransferase), AST (aspartate aminotransferase): < 4x IULN (institutional upper limit of normal)
  • Total bilirubin: </= 2.0 mg/dL
  • Creatinine: </= 2.0 mg/dL
  • EF (ejection fraction) measured by 2D-ECHO or MUGA (multiple gated acquisition) scan of >/= 45%
  • FEV1 (forced expiratory volume), FVC (forced vital capacity) and DLCD(diffusing capacity of lung for carbon monoxide) >/= 50% of predicted value (corrected to serum hemoglobin)
  • Women of child-bearing potential and men with partners of child-bearing potential must use adequate contraception prior to study entry and up to 30 days following treatment.

排除标准

  • Pregnant or breast feeding
  • Severe chronic obstructive pulmonary disease requiring oxygen supplementation
  • History of spontaneous pneumothorax
  • Active ear/sinus infection
  • Claustrophobia
  • HIstory of sinus or ear surgery, excluding myringotomy or ear tubes
  • History of seizures

结局指标

主要结局

Presence or absence of a treatment limiting toxicity

时间窗: Toxicity assessment occurs within 24hrs of treatment

Treatment limiting toxicities are defined as the occurrence of any of the following complications within 24hrs of treatment: seizure disorder, pneumothorax, death, irreversible grade III or any grade IV toxicity that is determined by the treating physician to be at least likely related to HBO therapy.

次要结局

  • Reduction in time to neutrophil recovery and engraftment post-cord blood transplant.(Daily measurement of neutrophil counts, up to 40 days post transplant.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验