ACellDREAM2Autologous Transplantation of Adipose Tissue Derived Mesenchymal Stroma/Stem Cells (ASC) for Critical Limb Ischemia Treatment
Autologous ASC (for Adipose-derived Stem/Stroma Cell)
Isquemia Crónica Amenazante del Miembro+6
+ Enfermedades Oclusivas Arteriales
+ Arteriosclerosis
Estudio de Tratamiento
Resumen
Fecha de inicio: 4 de marzo de 2020
Fecha en la que se inscribió al primer participante.This study focuses on a severe condition called Critical Limb Ischemia (CLI), which is the most advanced stage of atheroma, a disease that commonly affects the lower limb arteries in elderly people. CLI is characterized by rest pain or ischemic ulcers and has a serious prognosis, with only 20% of patients recovering within 12 months, regardless of treatment. The study aims to help patients with CLI who have limited or no options for revascularization, a currently validated treatment. It explores the potential of a specific type of stem cells, known as Adipose-derived Stem/Stroma Cells (ASC), which have shown promise in preclinical trials and phase I trials for aiding recovery from CLI. The study is a phase II, prospective, multicentric, open trial without comparison groups. It plans to enroll up to 43 patients who will receive an intramuscular injection of ASC. The primary goal is to evaluate the number of patients who are alive, have not undergone major amputation, and are free from CLI after six months. The study will also assess various secondary endpoints, including the number of new vessels in the treated limb, blood flow, wound healing, pain reduction, and potential adverse events like wound infection and irritative dermatitis. It will also measure certain proteins in blood samples and growth factors associated with mesenchymal stem cells.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 2 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria: * Patients over 18 years old, * Rest pain or ischemic ulcers /gangrene of the lower limb, present for at least 15 days, requiring analgesic absorption, with ankle pressures less than 70 mmHg or toe systolic pressure less than 50 mmHg or TcPO2 of less than 30 mmHg Patient with persistent CLI after revascularization will be included if : 1. they have severe cardiac, respiratory or renal disease who are at increased risk of complication from surgery or anesthesia, e.g. moderately severe or severe heart failure (NYHA class III or IV), severe or very severe Chronic Obstructive Pulmonary disease or severe renal disease (creatinine clearance \<30 mL/minute). OR 2. there is no option for endovascular or open surgery revascularization ; or poor option (defined by: need for an infra-popliteal by-pass without the availability of autologous great saphenous vein, need for use of great saphenous vein \<3 mm in diameter for tibial level bypass based on venous duplex ultrasound, or calcified or small (\<2 mm) distal target vessel, or open wound on the receiving site or infrapopliteal PAD) * Patients who signed the informed consent, * Patient affiliated to a social security system Exclusion Criteria: * History of cancer * Need of a major amputation (amputation at or above the ankle) within 2 weeks, * Ulcers with exposure of tendons, osteomyelitis, or clinically uncontrolled infection, * TcPO2 \<10 mmHg at rest and \< 30 mmHg sitting with legs dependent (very poor vascular reserve), * Patient under judicial protection, * Pregnant women, * Women of childbearing age without effective contraception. * Refusal of the patient to participate in the study, * Positive HIV-1 or 2, Human T Leukemia virus (HTLV)-1 or 2, Hepatite B Virus (HBV) (except vaccine profile), Syphilis (except inactive disease), or Hepatite C Virus (HCV) * Patients necessitating drugs with inhibitory or stimulatory effect on the growth and multiplication of cells or drugs with immunosuppressive effect: Cyclosporine, Mycophenolate mofetil, Azathioprine, Tacrolimus (systemic), Anthracyclines, Neupogen or equivalent, Etanercept, Interferons, Corticoids at anti-inflammatory doses. * No possibility of adipose tissue harvest and cell injection in the leg * Another clinical trial participation (except non interventional studies), * Patient under judicial protection, * Pregnant and breastfeeding women, * Women of childbearing age without effective contraception, * Lack in understanding the nature and aims of the study and/or difficulties in communication with the investigator.
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Un solo grupo de intervención está designado en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalObjetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene una ubicación