search
Back to results

Cold Plasma Therapy for Acceleration of Wound Healing in Diabetic Foot

Primary Purpose

Diabetic Foot

Status
Active
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Argon Plasma Jet
Placebo
Sponsored by
Ruhr University of Bochum
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 or Type 2 Diabetes mellitus
  • HbA1c ≤ 10%
  • at least one chronic wound persisting for at least three weeks without healing tendency following standard care wound therapy (Armstrong Wagner Grade Ib or IIb)

Exclusion Criteria:

  • concomitant wound treatment with local vacuum therapy or maggot therapy
  • dialysis
  • use of topical active antibiotics,
  • concomitant treatment with platelet rich fibrin,
  • presence of critical limb ischemia defined as ankle brachial index below 0.5 or transcutaneous oxygen pressure below 15 mmHg.
  • participation in another clinical trial
  • women of child bearing potential without effective contraception or active breastfeeding

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Sham Comparator

    Arm Label

    Plasma

    Placebo

    Arm Description

    regular treatment with Argon Plasma Jet according to manufacturer's instructions, 8 times within 14 days

    Sham-treatment with Argon Plasma Jet, Plasma producing electric field switched off - no Plasma is produced, just argon gas as effluent, 8 times within 14 days

    Outcomes

    Primary Outcome Measures

    change in wound surface area
    change in wound surface area within 14 days treatment
    change in signs of clinical infection
    change in clinical signs of infections as judged by the investigator
    change in microbial load
    change in microbial count, being evaluated by microbial culture

    Secondary Outcome Measures

    time to significant wound surface area change
    time to 10% reduction of wound surface compared to treatment start
    total wound surface change during treatment
    total wound surface change compared to treatment start
    time to change in wound infection
    change in wound infection over treatment
    changes in Quality of life (EQ5D questionnaire)
    Evaluation of life quality during (EQ5D questionnaire) treatment period via questionaire
    changes in Quality of life (SF12 questionnaire)
    Evaluation of life quality during (SF12 questionnaire) treatment period via questionaire
    treatment related side effects - formation of keloids
    question to evaluate potential side effects of the therapy: formation of keloids will be answered in a "yes" or "no" fashion and reported
    treatment related side effects - presence of skin irritation
    question to evaluate potential side effects of the therapy: presence of skin irritation will be answered in a "yes" or "no" fashion and reported
    treatment related side effects - local bleeding
    question to evaluate potential side effects of the therapy: local bleeding will be answered in a "yes" or "no" fashion and reported
    treatment related side effects - proliferative skin reaction
    question to evaluate potential side effects of the therapy: proliferative skin reaction will be answered in a "yes" or "no" fashion and reported

    Full Information

    First Posted
    December 12, 2019
    Last Updated
    March 28, 2023
    Sponsor
    Ruhr University of Bochum
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04205942
    Brief Title
    Cold Plasma Therapy for Acceleration of Wound Healing in Diabetic Foot
    Official Title
    Cold Plasma Therapy for Acceleration of Wound Healing in Superficial, Infected Diabetic Foot
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2023
    Overall Recruitment Status
    Active, not recruiting
    Study Start Date
    August 17, 2016 (Actual)
    Primary Completion Date
    April 20, 2019 (Actual)
    Study Completion Date
    April 30, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Ruhr University of Bochum

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Diabetic foot is a common complication of diabetes mellitus and requires specialized treatment. Wounds are characterized by persistent infection and chronic inflammatory processes, impeding well directed matrix remodelling and wound closure. Cold plasma applications have demonstrated beneficial effects on wound healing in several case reports. The investigator-initiated "Kaltplasma Wund (KPW)-Trial" was performed to prove beneficial effects of cold plasma in wound healing in a prospective, placebo-controlled, randomized bi-center study.
    Detailed Description
    Diabetic foot (DF) is a major complication in patients with diabetes leading to increased risk of hospitalization, lower limb amputation, and death, as well as a significant decrease in quality of life. During lifetime the risk for developing DF is assumed to be 25%; with 30% of DF resulting in lower limb amputation. If compared to general population people with diabetes have a 20-fold higher risk for amputation. Diabetes mellitus is the leading cause of lower limb amputation. Ulceration and impaired wound healing are commonly associated with common co-morbidities; the increased risk of infection amongst patients with diabetes is driving chronification and accounts for lack of wound healing. Non-thermal atmospheric pressure plasma has been proposed as a tool for various biological and medical applications relying on its capacity to reduce bacterial load in the wound and to initiate wound healing. Biological plasma effects are largely dependent on plasma-generated reactive species in the gas phase, which subsequently diffuse or react with proteins and lipids in cells or tissues. Thus, the objective of this placebo-controlled patient-blinded study was to show that application of cold plasma in addition to standard care treatment compared to placebo could accelerate wound healing in terms of more rapid and clinical meaningful wound surface regression. Wound closure progression and microbiological analysis were monitored time dependently to prove the effects. Patient's well-being and subjective perceptions were evaluated during treatment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetic Foot

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    65 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Plasma
    Arm Type
    Experimental
    Arm Description
    regular treatment with Argon Plasma Jet according to manufacturer's instructions, 8 times within 14 days
    Arm Title
    Placebo
    Arm Type
    Sham Comparator
    Arm Description
    Sham-treatment with Argon Plasma Jet, Plasma producing electric field switched off - no Plasma is produced, just argon gas as effluent, 8 times within 14 days
    Intervention Type
    Device
    Intervention Name(s)
    Argon Plasma Jet
    Intervention Description
    Cold Plasma (CP) therapy is applied in the first week of treatment on a daily schedule, in the second week CP is applied every second day. In total, 8 applications are performed with a one day schedule variance.
    Intervention Type
    Device
    Intervention Name(s)
    Placebo
    Intervention Description
    Sham Cold Plasma (sham-CP) (switched off Electric field, no plasma production, just gas) therapy is applied in the first week of treatment on a daily schedule, in the second week sham-CP is applied every second day. In total, 8 applications are performed with a one day schedule variance.
    Primary Outcome Measure Information:
    Title
    change in wound surface area
    Description
    change in wound surface area within 14 days treatment
    Time Frame
    treatment period of max 15 days
    Title
    change in signs of clinical infection
    Description
    change in clinical signs of infections as judged by the investigator
    Time Frame
    treatment period of max 15 days
    Title
    change in microbial load
    Description
    change in microbial count, being evaluated by microbial culture
    Time Frame
    treatment period of max 15 days
    Secondary Outcome Measure Information:
    Title
    time to significant wound surface area change
    Description
    time to 10% reduction of wound surface compared to treatment start
    Time Frame
    treatment period of max 15 days
    Title
    total wound surface change during treatment
    Description
    total wound surface change compared to treatment start
    Time Frame
    treatment period of max 15 days
    Title
    time to change in wound infection
    Description
    change in wound infection over treatment
    Time Frame
    treatment period of max 15 days
    Title
    changes in Quality of life (EQ5D questionnaire)
    Description
    Evaluation of life quality during (EQ5D questionnaire) treatment period via questionaire
    Time Frame
    treatment period of max 15 days
    Title
    changes in Quality of life (SF12 questionnaire)
    Description
    Evaluation of life quality during (SF12 questionnaire) treatment period via questionaire
    Time Frame
    treatment period of max 15 days
    Title
    treatment related side effects - formation of keloids
    Description
    question to evaluate potential side effects of the therapy: formation of keloids will be answered in a "yes" or "no" fashion and reported
    Time Frame
    treatment period of max 15 days
    Title
    treatment related side effects - presence of skin irritation
    Description
    question to evaluate potential side effects of the therapy: presence of skin irritation will be answered in a "yes" or "no" fashion and reported
    Time Frame
    treatment period of max 15 days
    Title
    treatment related side effects - local bleeding
    Description
    question to evaluate potential side effects of the therapy: local bleeding will be answered in a "yes" or "no" fashion and reported
    Time Frame
    treatment period of max 15 days
    Title
    treatment related side effects - proliferative skin reaction
    Description
    question to evaluate potential side effects of the therapy: proliferative skin reaction will be answered in a "yes" or "no" fashion and reported
    Time Frame
    treatment period of max 15 days
    Other Pre-specified Outcome Measures:
    Title
    treatment related side effects - formation of keloids
    Description
    descriptive evaluation of side effects within 5 years after Treatment (at 1, 2 and 5 years after start of treatment) question to evaluate potential side effects of the treatment: formation of keloids will be answered in a "yes" or "no" fashion and reported
    Time Frame
    within 5 years after start of treatment (at 1, 2 and 5 years after start of treatment)
    Title
    treatment related side effects - presence of skin irritation
    Description
    question to evaluate potential side effects of the therapy: presence of skin irritation will be answered in a "yes" or "no" fashion and reported
    Time Frame
    within 5 years after start of treatment (at 1, 2 and 5 years after start of treatment)
    Title
    treatment related side effects - local bleeding
    Description
    question to evaluate potential side effects of the therapy: local bleeding will be answered in a "yes" or "no" fashion and reported
    Time Frame
    within 5 years after start of treatment (at 1, 2 and 5 years after start of treatment)
    Title
    treatment related side effects - proliferative skin reaction
    Description
    question to evaluate potential side effects of the therapy: proliferative skin reaction will be answered in a "yes" or "no" fashion and reported
    Time Frame
    within 5 years after start of treatment (at 1, 2 and 5 years after start of treatment)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Type 1 or Type 2 Diabetes mellitus HbA1c ≤ 10% at least one chronic wound persisting for at least three weeks without healing tendency following standard care wound therapy (Armstrong Wagner Grade Ib or IIb) Exclusion Criteria: concomitant wound treatment with local vacuum therapy or maggot therapy dialysis use of topical active antibiotics, concomitant treatment with platelet rich fibrin, presence of critical limb ischemia defined as ankle brachial index below 0.5 or transcutaneous oxygen pressure below 15 mmHg. participation in another clinical trial women of child bearing potential without effective contraception or active breastfeeding
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Diethelm Tschoepe, Prof
    Organizational Affiliation
    Herz- und Diabeteszentrum NRW, Ruhr-Universität Bochum
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    no sharing of patient data planned, data are analysed locally
    Citations:
    PubMed Identifier
    35007358
    Citation
    Hiller J, Stratmann B, Timm J, Costea TC, Tschoepe D. Enhanced growth factor expression in chronic diabetic wounds treated by cold atmospheric plasma. Diabet Med. 2022 Jun;39(6):e14787. doi: 10.1111/dme.14787. Epub 2022 Jan 21.
    Results Reference
    derived
    PubMed Identifier
    32672829
    Citation
    Stratmann B, Costea TC, Nolte C, Hiller J, Schmidt J, Reindel J, Masur K, Motz W, Timm J, Kerner W, Tschoepe D. Effect of Cold Atmospheric Plasma Therapy vs Standard Therapy Placebo on Wound Healing in Patients With Diabetic Foot Ulcers: A Randomized Clinical Trial. JAMA Netw Open. 2020 Jul 1;3(7):e2010411. doi: 10.1001/jamanetworkopen.2020.10411. Erratum In: JAMA Netw Open. 2020 Oct 1;3(10):e2024427.
    Results Reference
    derived

    Learn more about this trial

    Cold Plasma Therapy for Acceleration of Wound Healing in Diabetic Foot

    We'll reach out to this number within 24 hrs