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Diabetic Foot clinical trials

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NCT ID: NCT02474381 Recruiting - Diabetic Foot Clinical Trials

Autologous Endothelial Progenitor Cells Treatment of Diabetic Foot

Start date: December 2012
Phase: N/A
Study type: Interventional

The vascular pathologic basis of diabetic foot include arterial obstruction and micro-circulation defects.The latest technology of arterial reconstruction can only rebuild blood flow of anterior,posterior tibial artery and peroneal artery.Endothelial progenitor cells have been proved to integrate into damaged vascular endothelium and improve vasculogenesis in vitro and in animal experiment.Therefore endothelial progenitor cells are supposed to improve the micro-circulation status of diabetic foot patients.In this trial,the investigators recuit diabetic foot patients with infrapopliteal arterial obstructive disease,treat them with autologous endothelial progenitor cells after intraluminal intervention,and observe the therapeutic efficacy comparing to single intraluminal intervention.

NCT ID: NCT02467998 Recruiting - Burns Clinical Trials

Negative Pressure Wound Therapy Registry

NPWTR
Start date: January 2005
Phase:
Study type: Observational [Patient Registry]

The goal of the Negative Pressure Wound Therapy Registry (NPWTR) for Wounds is to provide real world patient data from electronic health records submitted to meet Stage 2 Meaningful Use in order to understand the effectiveness and safety of various NPWT devices and methods among patients with chronic wounds and ulcers. Randomized, controlled trials to establish product efficacy routinely exclude patients with the co-morbid conditions common to patients seen in usual clinical practice and thus the results of these Randomized Controlled Trials (RCTs) tend to be non-generalizable. Little is known about the effectiveness of NPWT among typical patients. Patient registries are also ideal for assessing long term safety issues in these devices.

NCT ID: NCT02399826 Recruiting - Diabetic Foot Clinical Trials

Study of Amniotic Membrane Graft in the Management of Diabetic Foot Ulcers

Start date: March 2015
Phase: N/A
Study type: Interventional

This is comparison trial comparing human amniotic membrane to standard wound care for non healing diabetic foot wounds over a 12 weeks period

NCT ID: NCT02352480 Recruiting - Clinical trials for Diabetic Foot Ulcers

Effectiveness of Aurix Therapy in Diabetic Foot Ulcers

Start date: January 2015
Phase: N/A
Study type: Interventional

The aim of this trial is to demonstrate the effectiveness of complete wound healing in a prospective, open-label, randomized trial in which diabetic food ulcers (DFU) will be treated using Aurix plus Usual and Customary Care (UCC) and compared to a group receiving just UCC as provided in up to 100 U.S. wound centers

NCT ID: NCT02322554 Recruiting - Pressure Ulcer Clinical Trials

Cellular and Tissue Based Therapy Registry

CTPR
Start date: January 2005
Phase:
Study type: Observational [Patient Registry]

The goal of the Cellular and Tissue Based Therapy Registry (CTPR) for Wounds is to provide real world patient data from electronic health records submitted to meet Stage 2 Meaningful Use in order to understand the value of these products among patients with chronic wounds and ulcers. Randomized, controlled trials to establish product efficacy routinely exclude patients with the co-morbid conditions common to patients seen in usual clinical practice and thus the results of these RCTs tend to be non-generalizable. Little is known about the effectiveness of CTPs among typical patients.

NCT ID: NCT02312596 Recruiting - Clinical trials for Diabetic Foot Ulcers

A Prospective, Randomized Clinical Trial of PRP Concepts Fibrin Bio-Matrix in Non-Healing Diabetic Foot Ulcers

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

A prospective, randomized, controlled, clinical study to establish clinical based evidence of PRP Concepts Fibrin Bio-Matrix and compare its performance with the usual and customary practice for the treatment of Wagner 1 or 2 DFUs.

NCT ID: NCT02304588 Recruiting - Diabetic Foot Clinical Trials

Stem Cell Therapy for Patients With Vascular Occlusive Diseases Such as Diabetic Foot

Start date: January 2013
Phase: Phase 1
Study type: Interventional

Mesenchymal stem cells with multidirectional differentiation potential,autologous stem cell transplantation into ischemic foot, make its differentiation to form new blood capillary, improve and restore the local blood flow.

NCT ID: NCT02280733 Recruiting - Clinical trials for Peripheral Arterial Disease

A Real World, Observational Registry of Chronic Wounds and Ulcers

USWR
Start date: January 2005
Phase:
Study type: Observational [Patient Registry]

More than 100 hospital based outpatient wound centers in the USA and Puerto Rico agree to transmit structured data on all patients followed with chronic wounds and ulcers (e.g. diabetic foot ulcers, venous ulcers, pressure ulcers, arterial ulcers, surgical wounds, and traumatic wounds). Data are collected at point of care including adherence to wound care quality measures developed by the USWR as a Qualified Clinical Data Registry (QCDR).

NCT ID: NCT02087215 Recruiting - Diabetic Foot Ulcer Clinical Trials

Effect of Local Application of Boron on Diabetic Foot Ulcers

Start date: January 2014
Phase: Phase 1
Study type: Interventional

Boron as a naturally occurring element has some metabolic and inflammatory actions. The antibacterial activity against gram negative bacteria is also known. Boron deficiency is shown to be related with impaired wound bone healing in rats. Therefore, special wound care formulas containing boron may have some positive effect on wound healing of the patients with diabetic foot ulcers.

NCT ID: NCT02086955 Recruiting - Diabetic Foot Ulcer Clinical Trials

Outpatient Nurse Managed Counseling Program for Patients With Diabetic Foot Ulceration

Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the effectiveness of a nurse led intervention for high risk patients with diabetic foot ulceration and/or amputation. The effectiveness is defined in two ways 1) as a reduction in complication rates (time till ulceration recurrence, new ulcerations, amputation or reamputation) and 2) as a reduction in hospital readmissions for foot-related complication (one year survival probability: failure = readmission for ulceration recurrence, new ulcerations, amputation or re-amputation).