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TerminatedNCT01599442August-1Updated Apr 7, 2014

Register for Patients With Diabetic Foot Syndrome and Critical Limb Ischemia

An observational study in Type 2 Diabetes Mellitus, Diabetic Foot and Critical Limb Ischemia, sponsored by GWT-TUD GmbH. Terminated at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-04-07.

Sponsored by GWT-TUD GmbH · Observational

Why this study was terminated
recrution number was not reached
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
123
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

August-1 is a register 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.

02

Conditions studied

  • Type 2 Diabetes Mellitus
  • Diabetic Foot
  • Critical Limb Ischemia
03

In context

Diabetic Foot

1,054 studies on the registry are indexed under Diabetic Foot; 222 are open to participants now.

This study's enrollment of 123 is above the median of 100 across 186 observational studies indexed under Diabetic Foot.

Browse Diabetic Foot studies →

Lead sponsor

GWT-TUD GmbH is the lead sponsor of 39 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

outpatients from hospitals with a department specializing in the treatment of diabetic foot syndrome

Inclusion criteria

  • diabetic patients with dfs and critical limb ischemia
  • age 18 and older

Exclusion criteria

Exclusion Criteria:

  • less than 1 year life expectancy
  • prior major amputation
  • planned major expectation
  • prior treatment of the current episode of dfs with urokinase
  • mechanical heart valve replacement
  • cerebral event with changes in CT during the last three months
  • non-remediated proliferating retinopathy
  • uncontrolled hypertension (systolic > 180 mmHg, diastolic > 100 mmHg)
  • hemorrhagic diathesis (spontaneous quick value \< 50%, spontaneous ptt > 40 sec, thrombocytes \< 100 gpt/l)
  • acute gastrointestinal bleeding or ulcers during the last 4 weeks
  • prior reverse bypass operation
  • concomitant participation in other clinical trials
  • insufficient compliance
  • premenopausal women not using a safe method of contraception (i. e. IUD, hormone implants, hormone depot injection, combined pill (estrogens and gestagens), vaginal ring or vasectomized partner).
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
123 participants (actual)
06

What researchers measure

Primary outcomes

  1. duration of survival without major amputation

    Time frame: to be assessed after 12 months observation

Secondary outcomes

  1. major amputation

    Time frame: after 12 months observation

  2. total mortality

    Time frame: after 12 months observation

07

Study locations

1 site
  • Krankenhaus Dresden-Friedrichstadt
    Dresden, Sachse 01076, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 7, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01599442
Lead sponsor
GWT-TUD GmbH
Responsible party
Sponsor
First posted
May 16, 2012
Start date
Jun 2010
Primary completion
Jul 2013
Completion
Jul 2013
Last update
Apr 7, 2014

Study contacts

S. Schellong, Prof.Dr.med.
principal investigator · Staedt. KH Dresden-Friedrichstadt

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Apr 2014. You cannot join it, but the record below documents what was studied.

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