跳至主要内容
临床试验/NCT05576220
NCT05576220尚未招募不适用

Remote Temperature Monitoring of Adult Subjects Undergoing Outpatient Stem Cell Transplant or CAR-T Cell Therapy at Risk for Developing Infections and/or Cytokine Release Syndrome

IDION Inc.2 个研究点 分布在 1 个国家目标入组 210 人开始时间: 2023年4月30日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
210
试验地点
2
主要终点
To evaluate the IDION Shield remote subject temperature monitoring service.

研究概览

简要总结

IDION is currently seeking FDA approval for this device- the IDION iTempShield. It is a skin-safe, FDA complaint and non-invasive device that can read and monitor skin temperature. Having continuous temperature monitoring using the IDION iTempShield may provide early detection of a fever for patients with febrile neutropenia. Febrile neutropenic fever is common in patients receiving chemotherapy and can often indicate infection. The main potential benefit potenially experienced from participating in this study would be the early detection of fever.

There is a potential benefit that infection will be detected earlier in subjects wearing the IDION iTempShield.

详细描述

The purpose of the study is to evaluate the remote patient temperature monitoring service of the Idion Shield system in patients undergoing outpatient stem cell transplantation or CAR-T therapy who are at risk for developing infections and/or cytokine release syndrome. Febrile neutropenia remains a significant complication of treatment and often it is the first and sometimes the only sign or symptom of infection in this vulnerable patient population.

CAR-T patients are at risk for not only febrile neutropenia but also cytokine release syndrome (CRS), a systemic inflammatory response that can lead to hypoxia and shock. Fever is typically the first sign and hallmark of this potentially life-threatening condition. Routine measurement of body temperature is an important aspect of monitoring for signs of infection in patients receiving chemotherapy and for CRS in CAR-T patients.The current of standard of care for patients is to take their oral temperature when they feel ill and directing them to call their physician when their oral temperature reading is above 100.4. Having continuous temperature monitoring using the IDION iTempShield may provide early detection and intervention while reducing hospitalization rates, improving outcomes, and preventing death. With an increase in technological advancements and telemedicine, remote monitoring has shown to reduce health costs while providing closer follow-up for patients. The study will also analyze the potential reimbursement through Medicare to show the cost-benefit for remote monitoring utilizing the IDION iTempShield.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
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

  • Subject is being treated for a cancer diagnosis with a plan for outpatient transplant or CAR-T therapy
  • Subject is ≥ 18 years or older.
  • Subject is being treated or coming to the infusion center for clinical follow up every 2 weeks.
  • Subject has an iOS or Android phone.
  • Subject is willing to install the Idion app on his/her phone.
  • Subject self identifies as proficient in smart phone use.
  • Subject is willing to allow Idion to send text reminders to take temperature or complete surveys.
  • Subject is willing to configure the phone to ensure these notifications are delivered, even when phone is in a "no notification" mode.
  • Subject or subject caretaker is able and willing to complete subject surveys.
  • Subject is willing and able to provide written informed consent in English or Spanish.
  • Subject is willing and able to comply with all study procedures, requirements, assessments, visits, and complete questionnaires.

排除标准

  • Non-English or Spanish speakers
  • Unable to provide informed consent
  • Subjects with known adhesive allergy for silicon adhesives
  • Subjects with history of Medical Adhesive-Related Skin Injury (MARSI)
  • Subjects with no available

结局指标

主要结局

To evaluate the IDION Shield remote subject temperature monitoring service.

时间窗: 6 Months

The ability of the Idion System to transmit alerts if there is a temperature excursion sustained for at least 15 minutes above the alert protocol. There is a full data set time correlated with temp data in, battery voltage status and alerts that have been sent by Idion. The data will be mined and compared with the number of alerts and the timing of those alerts in the database.There will be times when the mobile device is offline due to mobile device battery exhaustion or distance traveled away from the device (left mobile at home) and these alerts will be missed.

次要结局

  • To assess subject and clinician satisfaction and compliance with the remote subject temperature monitoring service.(30 days)
  • To evaluate the clinical course of subjects with elevated temperatures(6 Months)

研究者

发起方
IDION Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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