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临床试验/NCT04255004
NCT04255004已完成不适用

Autologous Peripheral Blood Mononuclear Cells for Limb Salvage in Diabetic Foot Patients With No-option Critical Limb Ischemia

Ospedale San Donato0 个研究点目标入组 76 人开始时间: 2014年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
76
主要终点
Amputation-free survival at 1 month

研究概览

简要总结

The objective of this trial is to determine whether PBMNCs in diabetic patients with critical, non revascularizable limb ischemia can prevent major amputation and affect mortality and healing.

详细描述

This is an interventional study with historical control group carried out to assess as primary outcome major amputations, overall mortality, number of healed patients in group of patients who received repetitive intra-muscular implant of PBMNCs (3 times; 4-week interval) in comparison to a historical internal control group with a 1:1 case-control ratio. Secondary outcomes are TCPO2, healing time and rest pain.

No-option critical limb ischaemia is defined by evidence of no run-off pedal vessels, failure after several percutaneous intervention and no longer possible re-intervention, failure after infra-genicular bypass grafting, no-walking capacity with severe comorbidities unfit for surgical or endovascular procedures.

Inclusion criteria are: a) ulcers with inadequate perfusion, as indicated by a transcutaneous oxygen pressure value (TcpO2) <30 mmHg; b) ulcers with grade I or II or III and stage C as defined by the Texas University Classification System or W1,2,3 - I 3 - FI 0,1 as defined by the WiFI Classification System c) not eligible for angioplasty or vascular surgery or following failed revascularization; d) possibility to save foot support.

Exclusion criteria are: a) lesion site above the tibial-tarsal joint; b) moderate or severe infection according by the WiFI classification system; c) NYHA class IV; d) Anemia (Hb<8g/dl); e) coagulation disorder/thrombocytopenia (PLT< 50,000 per microliter); f) active cancer/leukemia or lymphoma hematological disease.

Standard of care in both groups includes: diabetes control maximization by the diabetologist, comprehensive foot assessment by the nurse together with the diabetologist, including determination of vibration perception threshold, 10-g monofilament test and TcpO2 measurement, dressings, off-loading and systemic therapy according to the IWGDF guidelines .

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ulcers with inadequate perfusion, as indicated by a transcutaneous oxygen pressure value (TcpO2) <30 mmHg;
  • ulcers with grade I or II or III and stage C as defined by the Texas University Classification System or W1,2,3 - I 3 - FI 0,1 as defined by the WiFI Classification System
  • not eligible for angioplasty or vascular surgery or following failed revascularization;
  • possibility to save foot support.

排除标准

  • lesion site above the tibial-tarsal joint;
  • moderate or severe infection according by the WiFI classification system;
  • NYHA class IV; d) Anemia (Hb<8g/dl);
  • coagulation disorder/thrombocytopenia (PLT< 50,000 per microliter);
  • active cancer/leukemia or lymphoma hematological disease.

结局指标

主要结局

Amputation-free survival at 1 month

时间窗: 1 month

rate of non amputated limb 1 month after the intervention

Amputation-free survival at 3 months

时间窗: 3 months

rate of non amputated limb 3 months after the intervention

Amputation-free survival at 6 months

时间窗: 6 months

rate of non amputated limb 6 months after the intervention

Amputation-free survival at 12 months

时间窗: 12 months

rate of non amputated limb 12 months after the intervention

Amputation-free survival at 18 months

时间窗: 18 months

rate of non amputated limb 18 months after the intervention

Amputation-free survival at 24 months

时间窗: 24 months

rate of non amputated limb 24 months after the intervention

risk of death at 1 month

时间窗: 1 month

rate of dead subjects 1 month after the intervention

risk of death at 3 months

时间窗: 3 months

rate of dead subjects 3 months after the intervention

risk of death at 6 months

时间窗: 6 months

rate of dead subjects 6 months after the intervention

risk of death at 12 months

时间窗: 12 months

rate of dead subjects 12 months after the intervention

risk of death at 18 months

时间窗: 18 months

rate of dead subjects 18 months after the intervention

risk of death at 24 months

时间窗: 24 months

rate of dead subjects 24 months after the intervention

probability of healing at 1 month

时间窗: 1 month

rate of healed subjects 1 month after the intervention

probability of healing at 3 months

时间窗: 3 months

rate of healed subjects 3 months after the intervention

probability of healing at 6 months

时间窗: 6 months

rate of healed subjects 6 months after the intervention

probability of healing at 12 months

时间窗: 12 months

rate of healed subjects 12 months after the intervention

probability of healing at 18 months

时间窗: 18 months

rate of healed subjects 18 months after the intervention

probability of healing at 24 months

时间窗: 24 months

rate of healed subjects 24 months after the intervention

次要结局

  • transcutaneous oxygen measurement (TcPO2) variation(0-3 months)
  • Healing time(within 24 months)
  • rest pain(0-1-3 months)

研究者

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

Alessia Scatena

Principal Investigator

Ospedale San Donato

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