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| Sponsor: | medac GmbH |
|---|---|
| Information provided by: | medac GmbH |
| ClinicalTrials.gov Identifier: | NCT00537498 |
Purpose
The purpose of this study is to evaluate whether a treatment with urokinase (500 000 or 1 000 000 IU) can lead to ulcer-healing, lower rate of major amputation, and prolonged survival in patients with diabetic foot syndrome.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetic Foot Arterial Occlusive Disease Ischemia |
Drug: Urokinase |
Phase II |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase II Study of Urokinase Therapy for Treatment of Angiopathic or Angioneuropathic Diabetic Foot Syndrome |
| Enrollment: | 77 |
| Study Start Date: | February 2002 |
| Study Completion Date: | December 2006 |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Interventional group
|
Drug: Urokinase
Daily intravenous application of urokinase over 30 minutes Dosage: If plasma fibrinogen is > 2,5g/l application of 1 000 000 IU Urokinase If plasma fibrinogen is < 2,5g/l application of 500 000 IU Urokinase If plasma fibrinogen is < 1,6g/l treatment must be stopped and continued after rising up to >2g/l |
Patients with diabetic foot ulceration and critical limb ischemia have a high risk of major amputation especially if limbs cannot be revascularized. Urokinase is effective in improving the microcirculation in critical limb ischemia by lowering fibrinogen and might improve outcomes. There are however no data on the efficacy and safety of urokinase treatment in terms of survival free of major amputation, ulcer healing and the rate of minor and major bleeding. Therefore this trial is conducted to investigate the effect of urokinase treatment on these parameters.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Germany | |
| Universitätsklinikum Carl Gustav Carus UniversitätsGefäßcentrum | |
| Dresden, Germany, 01307 | |
| Principal Investigator: | Sebastian M. Schellong, Professor | Universitätsklinikum Carl Gustav Carus TU Dresden UniversitätsGefäßcentrum |
More Information
| ClinicalTrials.gov Identifier: | NCT00537498 History of Changes |
| Other Study ID Numbers: | MC-UK.2/AVK |
| Study First Received: | September 28, 2007 |
| Last Updated: | March 24, 2010 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
|
urokinase, diabetes, wound healing, major amputation |
|
Arterial Occlusive Diseases Ischemia Diabetic Foot Vascular Diseases Cardiovascular Diseases Pathologic Processes Diabetic Angiopathies Foot Ulcer |
Leg Ulcer Skin Ulcer Skin Diseases Diabetes Complications Diabetes Mellitus Endocrine System Diseases Diabetic Neuropathies |