Plasma On Chronic Wounds for Epidermal Regeneration

N/AActive Not RecruitingNCT05855499

Coldplasmatech120 enrolled

Overview

Every year, 5 million people throughout Germany suffer from extensive, often chronic wounds. Cold plasma is an innovative therapeutic approach in the treatment of these persistent tissue defects. However, previous therapy options with cold plasma are very time-consuming, especially with increasing wound area, and are also strongly dependent on the skill of the practitioner. This study investigates the effectiveness of a system for reproducible application of cold plasma on larger areas and observes the effect of a 4-week additional plasma treatment on wound healing of large chronic wounds. The patient-related benefit of such an additional treatment will also be evaluated. Both study arms will receive guideline-based wound therapy, which is the current gold standard.

The clinical trial investigates the efficacy of an additional 4-week initial plasma therapy (CAPT) in direct comparison to standard guideline-based wound therapy (SWT) alone. The reactivation of healing of chronic, non-healing wounds will be assessed. This reactivation is primarily measured by the reduction of wound area, a valid and clinically accepted parameter for wound healing. A large number of RCTs and cohort studies demonstrate a strong correlation between the reduction in wound area at 4 weeks and the therapy outcome at 12 and 20 weeks. In addition to wound area reduction, other clinical parameters such as wound volume, wound closure, percentage of necrotic and fibrotic tissue, percentage of granulation tissue, wound exudate, and microflora are recorded. By recording these secondary endpoints, it is possible to closely track and analyse changes in wound condition induced by cold plasma. Another focus of the clinical trial is the evaluation of patient-related outcomes such as frequency of occurrence of infections, perception of pain, occurrence of adverse events, frequency of hospitalization, and change in quality of life. These events are fully documented to evaluate the safety of the treatment and to rule out potential risks.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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 study if it meets all inclusion criteria and no exclusion criteria and is suitable for use of the investigational product. The target wound is at least 2 cm away from the other wound(s) * The wound was diagnosed - at the time of planned inclusion - more than 8 weeks ago and 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 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/needing antiseptic/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 "basic monitoring": near-patient respiratory gas measurement (oxygen, carbon dioxide and inhalation 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 after debridement * The wound is undermined * The wound is located at the knee or above

Locations (8)

Universitäts-Hautklinik Tübingen

Tübingen, Baden-Wurttemberg, Germany

Zentrum Rothenaicher

München, Bavaria, Germany

Zentrum Regensburg

Regensburg, Bavaria, Germany

Universitätsklinikum Hamburg-Eppendorf

Hamburg, Free and Hanseatic City of Hamburg, Germany

Katholisches Klinikum Bochum

Bochum, North Rhine-Westphalia, Germany

Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden

Dresden, Saxony, Germany

Charité Universitätsmedizin Berlin

Berlin, State of Berlin, Germany

Verbund Thüringen-Kliniken "Georgius Agricola"

Saalfeld, Thuringia, Germany

Outcomes

Primary Outcomes

Change in area of chronic wounds

Chronic wound area is measured in square centimeters (cm²) using the SilhouetteStar® computer-assisted image-based wound measurement system. The outcome is the absolute change in wound area from baseline to Day 25, calculated as wound area at Day 25 minus wound area at baseline.

Time frame: 3 visits weekly for 4 weeks

Change from baseline in SF-12 Mental Component Summary score at Day 25

Mental health-related quality of life is measured using the Mental Component Summary score of the 12-Item Short Form Health Survey (SF-12). The outcome is the change in the SF-12 Mental Component Summary score from baseline to Day 25, expressed in points. The SF-12 scale ranges from 0 to 100, where 50 represents the population average and higher scores indicate a better health status.

Time frame: 3 visits weekly for 4 weeks

Secondary Outcomes

Wound closures

Number of participants with wound closure during the 4-week active treatment phase and at the 3-month and 6-month follow-up assessments.

Time frame: during the 4-week active treatment phase, after 3 and after 6 months

Change in wound pain

Change in wound pain during activity or at rest during the 6-month observation period. Pain was assessed using an NRS with values ranging from 0 to 10. Higher scores indicate worse pain.

Time frame: during the 6-month observation period

Change in the amount of germs/bacteria in the wound bed

For this purpose, swabs are taken before and after treatment. The swabs are then examined in the laboratory with regard to the microflora (germ type and resistance). The bacterial load is measured on a logarithmic scale. Lower values indicate a lower bacterial load and therefore a better outcome.

Time frame: during the 4-week active treatment phase