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Diabetic Foot clinical trials

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NCT ID: NCT01729286 Terminated - Clinical trials for Foot Ulcer, Diabetic

Health Economic Assessment of Lower Extremity Diabetic (HEALED) Ulcers With PriMatrix

HEALED
Start date: September 2012
Phase: N/A
Study type: Interventional

The objective of this study is to compare the effectiveness of PriMatrix Moist Wound Therapy (MWT) with Standard of Care MWT for the treatment of chronic diabetic foot ulcers in subjects with diabetes mellitus and without significantly compromised arterial circulation.

NCT ID: NCT01657318 Terminated - Diabetic Foot Clinical Trials

Olivamine-containing Products in the Management of Patients With Nonhealing Lower Extremity Ulcers

Start date: September 1, 2012
Phase:
Study type: Observational

In this study, the investigators hypothesize that the use of olivamine-containing products in the management of patients with compromised nonhealing lower extremity ulcers is feasible in the Philippine setting. It will result in complete ulcer healing or wound closure after 16 weeks.

NCT ID: NCT01638585 Terminated - Diabetic Foot Clinical Trials

Safety and Efficacy Study of Urokinase for the Treatment of Diabetic Foot Syndrome and Critical Limb Ischemia

August2
Start date: June 2011
Phase: Phase 3
Study type: Interventional

In this randomized clinical trial (RCT) the investigators are trying to find out whether a low-dose therapy with daily short infusions of urokinase using 10 to 21 doses over a maximum of 30 days is capable of prolonging the survival time without major amputation.

NCT ID: NCT01608776 Terminated - Diabetic Foot Ulcer Clinical Trials

RESPOND Restoring Equilibrium and Wound Stimulation to Promote Healing Of Non-healing DFUs

Start date: May 2012
Phase: Phase 4
Study type: Interventional

To evaluate the safety and effectiveness of MIST Therapy in conjunction with Standard of Care (SOC) compared to Standard of Care alone in the treatment of diabetic foot ulcers (DFU).

NCT ID: NCT01599442 Terminated - Clinical trials for Type 2 Diabetes Mellitus

Register for Patients With Diabetic Foot Syndrome and Critical Limb Ischemia

August-1
Start date: June 2010
Phase: N/A
Study type: Observational

Diabetic foot syndrome (DFS) is a disease caused by neurogenic (concerning the nervous system), vascular, mechanic and metabolic factors, which are further complicated by an impairment of the immune system and a corresponding increase in the risk for infections. Results from clinical trials about the efficacy of interventions aimed at reducing the number of patient-relevant end points are of limited comparability due to the heterogenity of patient characteristics. By their very nature, randomized clinical trials (RCT) can only focus on a limited section of the wide range of possible intervention regimes. In clinical practice, however, a number of patients with dfs will never have been part of a clinical trial. Furthermore, there are only very few contemporary registers for this indication from which conclusions with regard to the comparative merits of different therapeutic strategies may be drawn. The register was conceived to find out to which extent RCT patients are representative for the overall patient collective with dfs and critical limb ischemia and to evaluate the therapeutic success of other treatment strategies. An RCT to assess the efficacy of urokinase versus placebo is imbedded in the register.

NCT ID: NCT01573897 Terminated - Sleep Apnea Clinical Trials

Impact of Sleep Apnea on Diabetic Foot Wound.

SAS-FOOT
Start date: June 4, 2012
Phase:
Study type: Observational

Sleep apnea syndrome (SAS) is a common comorbidity of type 1 and type 2 diabetes. A low transcutaneous oxygen tension (PtcO2) measured on the foot is pejorative prognostic factor for the healing of a diabetic foot wound. SAS causes intermittent nocturnal hypoxia and sympathetic overactivity. The investigators hypothesized that SAS could be a factor reducing the PtcO2.Therefore, the main objective of this study is to assess the variation in PtcO2 between the end of the night and midday in patients with -or at risk of- diabetic foot wound according to the presence or not of sleep apnea syndrome.The secondary objective is to address the microvascularisation of diabetic patients having foot wounds according to their status regarding sleep apnea syndrome.

NCT ID: NCT01539811 Terminated - Clinical trials for Diabetic Foot Infections

Diabetic Foot Infection Antibiotic Study

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

This is a pilot study to explore the effects of long-course versus short course antibiotics on wound healing in surgically managed diabetic foot infections. Hypothesis: Diabetic Foot Infections (DFIs) are best managed with an early aggressive surgical approach and short term antibiotic use. Post-operative prolonged antibiotic use increases costs and resource utilization without improving outcomes.

NCT ID: NCT01531517 Terminated - Diabetic Foot Ulcer Clinical Trials

Study of the Efficacy of PedyPhar® Ointment on the Diabetic Foot Ulcers

PED111
Start date: July 2011
Phase: Phase 3
Study type: Interventional

Clinical Trial Phase III-b Study Sponsor: European Egyptian Pharmaceutical Industries Sample Size: 120 patients (60 per arm) Study Population: Patients with Diabetic foot ulcer of any stage after proper surgical treatment - if needed. Those patients will be recruited from patients attending the Diabetic foot Center at Faculty of Medicine - Alexandria University and the outpatient clinic at Faculty of Medicine, Cairo University. Recruitment Period: 9 months Dose application: thick layer of 2-3 mm applied to the dressing then dressing applied to the ulcer. Endpoints: Complete healing of the ulcer OR 5 months of application of the ointment whichever comes first

NCT ID: NCT01350102 Terminated - Clinical trials for Foot Ulcer, Diabetic

The Relationship of Hemoglobin A1c and Diabetic Wound Healing

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the relationship of hemoglobin A1c in diabetic wound healing. Additionally, a comparison of two wound dressings, AmeriGel® (Amerx Health Care Corp., Clearwater, FL) and Bacitracin, with and without vitamin C supplementation, will be done to evaluate impact on time to wound closure.

NCT ID: NCT01322256 Terminated - Osteoarthritis Clinical Trials

PET/CT Scanning for the Follow-up of Antibiotic Treatment of Infectious Osteoarthritis in the Diabetic Foot

ISEOD
Start date: October 2012
Phase: N/A
Study type: Interventional

The investigators' primary objective is to assess the predictive power of PET/CT scanning in the evolution of infectious osteoarthritis of the diabetic diabetic after antibiotic therapy prescribed by national and international recommendations.