ACellDREAM2Autologous Transplantation of Adipose Tissue Derived Mesenchymal Stroma/Stem Cells (ASC) for Critical Limb Ischemia Treatment
Autologous ASC (for Adipose-derived Stem/Stroma Cell)
Ischémie chronique menaçant le membre+10
+ Artériosclérose
+ Maladies Occlusives des Artères
Étude thérapeutique
Résumé
Date de début de l'étude : 4 mars 2020
Date à laquelle le premier participant a commencé l'étude.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.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.2 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 18 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
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 l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.Un seul groupe d'intervention est désigné dans cette étude
Cette étude ne comporte pas de groupe placebo.
Groupes de traitement
Groupe I
ExpérimentalObjectifs de l'étude
Objectifs principaux
Objectifs secondaires
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 1 site