Effectiveness of Measuring Local Tissue Oxygen in Response to Induced Hemodynamic Changes With the Profusa's Wireless Lumee Oxygen Platform in Patients With Peripheral Artery Disease (PAD)
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 53
- 试验地点
- 6
- 主要终点
- Correlation of subcutaneous oxygen dynamics measured by the Wireless Lumee Oxygen Platform and a TcPO2 device in the arm
研究概览
简要总结
The purpose of this study is to monitor changes in local tissue oxygen levels in participants with Peripheral Artery Disease (PAD) using the Wireless Lumee Oxygen Platform. A transcutaneous oxygen pressure (TcPO2) device is used to show correlations in oxygen dynamics. Oxygen dynamics are induced by a pressure cuff and position maneuvers. Study participants will participate in the study for 12 months with six (6) planned visits over the course of the study.
The investigational device, the Wireless Lumee Oxygen Platform, consists of the Lumee Oxygen, a sterile soft injectable oxygen-sensitive hydrogel, designed to sense and report oxygen levels in the subcutaneous tissue. After initial insertion of the hydrogel in the subcutaneous tissue using the Lumee Pen (a sterile disposable injector device), tissue oxygen levels can be monitored continuously using the Lumee Patch (a non-invasive, non-sterile, wireless electronic device to collect, analyze and report tissue oxygen levels sensed by Lumee Oxygen Hydrogel) attached to the skin through the Lumee Patch Adhesive (designed to adhere the Lumee Patch). The Lumee Patch sends collected tissue oxygen data to the Lumee App which displays the collected data and operates up to four Lumee Patches.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 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
- 否
入选标准
- •A suitable candidate must meet the following criteria:
- •Male or female must be ≥ 18 years of age
- •Diagnosed with PAD, stable at time of enrollment, and may include prior stable lower extremity revascularization
- •Has been informed of the nature of the study, agrees to its provisions, and has signed the informed consent form prior to any study related procedure
- •Should plan to be available for all safety follow-up examinations at the investigational site
- •Is aware that the Lumee™ Oxygen hydrogels are intended to stay in the tissue indefinitely
- •Is aware that photos of injection sites and wound site will be taken, and videos may be recorded
排除标准
- •A candidate will be excluded from the study if any of the following criteria are met:
- •PAD of Rutherford Classification 5 or 6 at time of enrollment
- •Subject has an active infection
- •Subject has an open wound on limb included in study
- •Known history of keloids, excessive fibrosis during wound healing
- •Known allergies to Lumee™ Oxygen hydrogel components, local anesthetic agents, suture materials, or severe skin allergies to adhesives
- •Any skin or musculoskeletal condition or deformity limiting injection of the Lumee™ Oxygen hydrogel or preventing subsequent attachments of the Lumee™ Patch system
- •Any skin modification in the area of injection that would potentially influence device performance (for example tattoos or scars)
- •Previous amputation proximal to the digital level on the limb included in the study
- •Significant venous insufficiency resulting in swelling of the lower leg, ankle or foot or chronic venous stasis changes (CEAP clinical score ≥ 3)
- •Any condition that at the discretion of the investigator, physician or designee will impact the safety of the subject or the scientific integrity of the trial
- •Female subjects of childbearing capacity (not surgically sterile or menopausal for ≥ 1 year)
- •Participation in another clinical study, that would potentially interfere with the participation in this study
- •Subject requires dialysis
- •Subject is immunocompromised
- •Subject has incompressible arteries tested by occlusion test in the arm
- •Inability to obtain consent
结局指标
主要结局
Correlation of subcutaneous oxygen dynamics measured by the Wireless Lumee Oxygen Platform and a TcPO2 device in the arm
时间窗: At 2 days (±1 day) after injection and at 3 months (±14 days) after injection
Correlation of measurements between subcutaneous tissue oxygen concentration expressed by the Lumee Oxygen Index (LOI; unitless; measured by the Wireless Lumee Oxygen Platform) and transcutaneous partial pressure of oxygen (TcPO2; mmHg; measured by the Periflux System 5000 or Periflux System 6000) in the arm during changes of oxygen induced by pressure cuff.
次要结局
- Correlation of subcutaneous oxygen dynamics measured by the Wireless Lumee Oxygen Platform and a TcPO2 device in the foot(1-14 days after hydrogel insertion)