Diabetic Foot Clinical Trial
Official title:
Study on Induced Wound Healing Through Application of Expanded Autologous Bone Marrow Stem Cells in Diabetic Patients With Ischemia-induced Chronic Tissue Ulcers Affecting the Lower Limbs
Diabetic foot patients with chronic limb ischemia and without the option for surgical or interventional revascularization were recruited and randomized to the transplant groups or the control group within this clinical trial. These patients are randomized to control or intervention group, whereas the intervention is divided into bone marrow cells administered intramuscular or intraarterial or expanded bone marrow cells administered intramuscular or intraarterial resulting in five distinct groups. To measure the therapeutic effects of the various treatment arms patients were evaluated for (ankle brachial index (ABI), transcutaneous oxygen partial pressure (TcPO2), and reactive hyperemia (Blood Oxygen Level Dependent [BOLD]). Patients also underwent imaging with angiographic methods.
Diabetic foot (DF) is a concomitant illness of diabetes mellitus. Diabetes is one of the
main causes of non-traumatic amputation worldwide due to severe peripheral arterial
occlusive disease with chronic critical limb ischemia being the most abundant problem.
Ulceration occurs as failure of oxygenation, nutrient supply and progressive occlusion of
larger blood vessels often exacerbates pre-existing microvascular abnormalities.
Purified bone marrow mononuclear cells or expanded bone marrow cells enriched in Cluster of
Differentiation 90+ (CD90+) mesenchymal stem cells (named tissue repair cells, [TRCs]) are
used in the treatment of diabetic ulcers in comparison to bone marrow derived stem cells to
induce revascularization of the affected limb and to enhance local perfusion. Cells are
administered intramuscular or intraarterial. A control group of patients treated according
national guidelines without stem cells serves as comparator.
Diabetic foot patients with chronic limb ischemia and without the option for surgical or
interventional revascularization were recruited and randomized to the transplant groups or
the control group within this clinical trial. To measure the therapeutic effects of the
various treatment arms patients were evaluated for (ankle brachial index (ABI),
transcutaneous oxygen partial pressure (TcPO2), and reactive hyperemia (Blood Oxygen Level
Dependent [BOLD]). Patients also underwent imaging with angiographic methods.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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