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
About this trial
This is an interventional treatment trial for Diabetic Foot
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
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
NCT ID
NCT04205942
First Posted
December 12, 2019
Last Updated
March 28, 2023
Sponsor
Ruhr University of Bochum
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
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