Shockwave Treatment of Diabetic Foot Ulcer: Step I

Not Applicable

Withdrawn

• Conditions: Chronic Diabetic Foot Ulcers
• Interventions: Procedure: Extracorporeal Shock Wave

• Registration Number: NCT00954343
• Lead Sponsor: Technical University of Munich

Brief Summary

Extracorporeal Shock Wave treatment is a well established treatment in orthopedics. Considerable success has been reported after treatment of various soft tissue pathologies (Tendinitis, heel spur etc). In recent years, encouraging results have been reported concerning the effect of the shock-wave on chronic wounds. It has been reported that healing time can be considerably shortened if shock-waves are applied to the wound in addition to conventional wound treatment. Yet, randomized, controlled, prospective trials are missing.

In this study, the effect of shock-waves on diabetic foot ulcer shall be assessed.

The study is composed of 5 groups of which 4 groups receive shock wave treatments (each with a different protocol). One group serves as an untreated control group. All groups get standardized wound treatment and wound dressing.

That shock-wave application protocol that shows the best results (rate of completely healed ulcer, most decrease of ulcer size) shall be tested in a further, sufficiently dimensioned, two-armed, randomized controlled trial (RCT).

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2009-07-31
• Study Start: 2009-08
• Study First Submitted QC: 2009-08-06
• Study First Posted: 2009-08-07
• Status Verified: 2013-03
• Last Update Submitted: 2013-03-18
• Last Update Posted: 2013-03-19

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Age 18 and older
• Diabetes Type I or II
• Chronic ulcer on the foot
• Ulcer present for at least 6 weeks
• Wagner Grade 1 or 2

Exclusion Criteria

• Chronic rest pain
• Critical ischemia
• Gangrene
• Ankle-Arm-Index < 0,5
• Critical ischemia treated within 6 weeks before possible enrollment
• Ulcer of Grade 3 or worse according to the Wagner Classification
• Osteomyelitis
• Affection of toes
• Necessity of surgical intervention
• Malalignment of the foot sustaining the ulcer
• Treatment of Ulcer with Prostaglandins or vasodilatators within the last 2 weeks
• Current therapy with corticoids
• Infection with HIV; Hepatitis
• Suppression of immune system (due to illness or medication)
• Medication with Vitamin-K-Antagonists
• Known hemophilia
• Sever Hypalbuminemia < 2 g/dl
• Severe anemia
• Ulcer other than of diabetic origin
• Pregnant or breast-feeding women
• Known coagulopathies
• Implants such as artificial heart valves, joint replacement, bone replacement, osteosynthesis material
• Patients participating on other studies
• Chemotherapy within the last 60 days
• Mentally disabled patients

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group III	Extracorporeal Shock Wave	-
Group II	Extracorporeal Shock Wave	-
Group IV	Extracorporeal Shock Wave	-
Group I	Extracorporeal Shock Wave	-

Primary Outcome Measures

Name	Time	Method
Percentage decrease of ulcer size twelve weeks after treatment begin (i.e. first shock wave treatment) compared to the baseline (ulcer size at first treatment)

Secondary Outcome Measures

Name	Time	Method
Rate of completely healed ulcer 6, 9 and 12 weeks after first treatment
Percentage decrease of ulcer size 6 and 9 weeks after first treatment
Tissue oxygen concentration after shock wave treatment

Trial Locations

Locations (1)

Klinik für Orthopädie und Unfallchirurgie, Klinikum rechts der Isar; 🇩🇪 Munic, Bavaria, Germany