Objectives: Demonstrate the safety and effectiveness of highly purified CD133+ autologous stem cells in critical limb ischemia (CLI). Design: Prospective single-center not randomized. Clinicaltrials.gov identifier: NCT01595776 Methods: Eight patients with a history of stable CLI were enrolled in a period of 2 years. After bone marrow stimulation and single leukapheresis collection, CD133+ immunomagnetic cell selection was performed. CD133+ cells in buffer phosphate suspension was administered intramuscularly. Muscular and arterial contrast enhanced ultra sound (CEUS), lesion evolution and pain management were assessed preoperatively and 3, 6 and 12 months after the implant. Results: No patient had early or late complications related to the ...
Background: Peripheral blood mononuclear cells (PBMNCs) and purified CD34+ cells (PCCs) are increasi...
PhD Aims: The aim of our study was to evaluate an efficacy and safety of intra-arterial injection of...
Objective—The purpose of this phase I open label non-randomized trial was to assess the safety and e...
Objectives: Demonstrate the safety and effectiveness of highly purified CD133+ autologous stem cells...
Additional file 1: Figure S1. The procedure of implant through multiple intramuscular 1 ml injection...
We report the safety and feasibility of autologous CD133þ cell implantation into the lower extremity...
Background: Stem cell therapy has been proposed to enhance the salvage of critically ischemic limbs....
INTRODUCTION: Critical Limb Ischemia (CLI) patients have a poor prognosis despite they are submitted...
Background: The therapeutic efficacy of bone marrow mononuclear cells (BM-MNC) autotransplantation i...
Objective. Critical limb ischemia (CLI) is the most dangerous stage of peripheral artery disease (PA...
ObjectiveThe purpose of this Phase I open label nonrandomized trial was to assess the safety and eff...
Abstract Critical limb ischemia (CLI) is a debilitating condition for which limited therapeutic opti...
International audienceBackground: Cell therapy has been proposed for patients with critical limb isc...
BackgroundThis study investigated the efficacy and safety of autologous bone marrow-mononuclear cell...
Objectives: The safety and efficacy of direct intramuscular injections of aldehyde dehydrogenase bri...
Background: Peripheral blood mononuclear cells (PBMNCs) and purified CD34+ cells (PCCs) are increasi...
PhD Aims: The aim of our study was to evaluate an efficacy and safety of intra-arterial injection of...
Objective—The purpose of this phase I open label non-randomized trial was to assess the safety and e...
Objectives: Demonstrate the safety and effectiveness of highly purified CD133+ autologous stem cells...
Additional file 1: Figure S1. The procedure of implant through multiple intramuscular 1 ml injection...
We report the safety and feasibility of autologous CD133þ cell implantation into the lower extremity...
Background: Stem cell therapy has been proposed to enhance the salvage of critically ischemic limbs....
INTRODUCTION: Critical Limb Ischemia (CLI) patients have a poor prognosis despite they are submitted...
Background: The therapeutic efficacy of bone marrow mononuclear cells (BM-MNC) autotransplantation i...
Objective. Critical limb ischemia (CLI) is the most dangerous stage of peripheral artery disease (PA...
ObjectiveThe purpose of this Phase I open label nonrandomized trial was to assess the safety and eff...
Abstract Critical limb ischemia (CLI) is a debilitating condition for which limited therapeutic opti...
International audienceBackground: Cell therapy has been proposed for patients with critical limb isc...
BackgroundThis study investigated the efficacy and safety of autologous bone marrow-mononuclear cell...
Objectives: The safety and efficacy of direct intramuscular injections of aldehyde dehydrogenase bri...
Background: Peripheral blood mononuclear cells (PBMNCs) and purified CD34+ cells (PCCs) are increasi...
PhD Aims: The aim of our study was to evaluate an efficacy and safety of intra-arterial injection of...
Objective—The purpose of this phase I open label non-randomized trial was to assess the safety and e...