Phase
Condition
Venous Leg Ulcers
Ulcers
Treatment
CPtcube, CPTpatch
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Inclusion criteria are divided into patient-specific and wound-specific criteria.
Patient Criteria:
Patient must be at least 18 years old (legal age) and legally competent
The patient has at least one diagnosed chronic (existing for at least 8 weeks),non-healing wound due to a UCA or UCV on the lower leg, below the knee
There is a signed consent form dated by the patient's own hand
Wound Criteria:
In case of multiple wounds, the largest wound by area will be included in the studyif it meets all inclusion criteria and no exclusion criteria and is suitable for useof the investigational product. The target wound is at least 2 cm away from theother wound(s)
The wound was diagnosed - at the time of planned inclusion - more than 8 weeks agoand classified as a chronic wound
The initial wound area is 5 cm²-100 cm2
The wound can be enclosed completely by the plasma applicator (10 cm x 10 cm)
The wound is not undermined
The wound is located on the lower leg
Exclusion
Exclusion Criteria:
The exclusion criteria are divided into patient-specific and wound-specific criteria.
Patient Criteria:
The patient is younger than 18 years and/or lacks legal capacity
The patient has already participated in this study
The patient is already participating in another interventional study
Pregnant or breastfeeding patients
The patient has an implanted pacemaker, defibrillator or other active implants
The patient has a light/sun allergy
The patient has a silicone allergy
The patient has had a thrombosis within the last 3 months
The patient has a systemic and/or chronic infectious disease (e.g., HIV,tuberculosis, hepatitis)
The patient has a tumour disease
An ongoing or recently completed chemotherapy or radiotherapy
The patient is undergoing severe endogenous or drug immunosuppression
The patient is receiving systemic antibiotic treatment or is receiving/needingantiseptic/antibiotic wound therapy in/near the wound
The patient does not have the necessary revascularization (paVK)
The patient requires vital instrumental monitoring in the sense of "basicmonitoring": near-patient respiratory gas measurement (oxygen, carbon dioxide andinhalation anaesthetic), pulse oximeter, ECG monitoring, blood pressure measurement (non-invasive), an oscillometric blood pressure measurement with automatic mode
Existing alcohol or drug abuse
The patient requires dialysis
Wound Criteria:
The wound is not a chronic wound as defined by study protocol
The wound is difficult to access or close to exposed vessels
The wound is critically colonized or infected
Acute infections in the wound area (radius 5 cm)
The wound is bleeding profusely. This does not include bleeding immediately afterdebridement
The wound is undermined
The wound is located at the knee or above
Study Design
Study Description
Connect with a study center
Universitäts-Hautklinik Tübingen
Tübingen, Baden-Württemberg 72076
GermanySite Not Available
Zentrum Rothenaicher
München, Bayern 81927
GermanySite Not Available
Zentrum Regensburg
Regensburg, Bayern 93047
GermanySite Not Available
Katholisches Klinikum Bochum
Bochum, Nordrhein-Westfalen 44805
GermanySite Not Available
Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden
Dresden, Sachsen 01307
GermanySite Not Available
Verbund Thüringen-Kliniken "Georgius Agricola"
Saalfeld, Thueringen 07318
GermanySite Not Available
Charité Universitätsmedizin Berlin
Berlin, 10117
GermanySite Not Available
Universitätsklinikum Hamburg-Eppendorf
Hamburg, 20246
GermanySite Not Available
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