跳至主要内容
临床试验/jRCT1032230294
jRCT1032230294招募中不适用

Comprehensive analysis-driven identification of mechanisms and biomarkers of therapeutic apheresis to cure ulcer in peripheral arterial disease study (CURE-PAD study)

Kaneka Corporation0 个研究点目标入组 6 人开始时间: 2022年12月5日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
6
主要终点
Changes in the scores of the ulcer before and after apheresis therapy

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • Part 1: Patients who meets all of the criteria lisited below:
  • Patients who were diagnosed with arteriosclerosis obliterans.
  • Patients with lower limb lesion of Fontaine classification IV (ulcers and/or gangrene).
  • Patients who has lesions refractory to conventional pharmacotherapies and are unable or difficult to undergo revascularization by percutaneous transluminal angioplasty (PTA) or vascular surgery according to the attached document and/or practical guide of Rheocarna.
  • Patients who can provide written informed consent. If the patients are not able to provide informed consent, the representative can provide written informed consent.
  • Patients who had participated in the LDL Apheresis-Mediated Endothelial Activation Therapy to Severe Peripheral Artery Disease (LETS-PAD) study (jRCTs032180100) and had lower limb lesions of Fontaine classification IV (ulcers and/or gangrene) and gave permission for secondary use of samples and information.

排除标准

  • Part 1: Patients who meets all of the criteria lisited below:
  • Patients who undergo any of the therapies listed below during the aferesis sessions:
  • a) Any other apheresis therapies (regardless of reasons)
  • Patients whose doctor diagnosed that apheresis therapy is not indicated according to the attached document and/or practical guide of Rheocarna.
  • Patients who denied permission for secondary use of samples and information.

结局指标

主要结局

Changes in the scores of the ulcer before and after apheresis therapy

The size, severity of inflammatory/infectious lesions, proportions of granulation tissue, and severity of necrotic lesions of the ulcer are evaluated according to DESIGN-R. One ulcer is chosen for assessment of therapeutic effects.

Changes in proteins and metabolites in blood samples before and after apheresis therapy

Proteomic (and metabolomic analyses in Part 2) are conducted on blood samples to measure proteins and metabolites comprehensively. Changes in the measurements of each biomarker before and after apheresis therapy are calculated.

次要结局

未报告次要终点

研究者

相似试验