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Diabetic Foot Ulcers (DFU)PROSPECTNCT07073040

Efficacy and Safety of Cold Atmospheric Plasma Combined With Endovascular Intervention in Patients With Diabetic Foot Ulcers and Lower Extremity Arterial Occlusion

A study testing Cold atmospheric plasma (CAP) and Successful infrapopliteal angioplasty in people with Diabetic Foot Ulcers (DFU) and Lower Extremity Arterial Occlusion, run by Shenyang Medical College at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Critical limb ischemia is the end-stage manifestation of peripheral arterial disease (PAD), frequently presenting as ischemic rest pain, ulceration, or gangrene. Diabetes mellitus is a major risk factor for lower extremity arterial occlusion, with infrapopliteal arteries most commonly affected. Read more about this study

Who is it for?
Ages 18 to 80 years
What is being tested?
Cold atmospheric plasma (CAP) and Successful infrapopliteal angioplasty
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
86 participants
Where
1 siteChina
Study dates
22 Jul 2025to 6 May 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Aged 18-80 years, with a diagnosis of type 1 or type 2 diabetes and diabetic foot ulcer; glycated hemoglobin (HbA1c) ≤ 10%.
  • Presence of at least one chronic foot ulcer persisting for at least three weeks, with no signs of healing after standard-of-care treatment based on current clinical guidelines. The ulcer must be classified as Wagner-Armstrong grade 1D or 2D (Wagner: superficial ulcer [grade 1] or ulcer extending to tendon [grade 2]; Armstrong: presence of both ischaemia and infection [stage D]).
  • Documented infrapopliteal arterial stenosis or occlusion by vascular ultrasound and/or CT angiography (CTA), meeting indications for revascularization. All enrolled patients must have received successful infrapopliteal balloon angioplasty, with intraoperative angiography confirming target artery patency.
  • Provision of written informed consent.

Who cannot join

  • Concurrent treatment of the wound with local vacuum therapy or maggot therapy.
  • Undergoing dialysis.
  • Use of local active antibiotics.
  • Treatment with platelet-rich fibrin.
  • Women of childbearing potential without effective contraception, or women who are actively breastfeeding.
  • Presence of other severe organ dysfunction, with an expected survival of less than six months.
  • Participation in another clinical trial within the past three months or currently enrolled in another clinical trial.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Yun-En Liu, MD contact

86-24-62215130

lye9901@163.com

China1 site, 1 recruiting
  • Ansteel General Hospital

    Anshan, Liaoning

    Dong-ming Ren, MM, 86-13352107771, rendongminganshan@163.com

    Recruiting

Other trials in China

About this study

Official title: Efficacy and Safety of Cold Atmospheric Plasma Combined With Endovascular Intervention in Patients With Diabetic Foot Ulcers and Lower Extremity Arterial Occlusion: a Randomized, Double-blind, Placebo-controlled Clinical Trial

Critical limb ischemia is the end-stage manifestation of peripheral arterial disease (PAD), frequently presenting as ischemic rest pain, ulceration, or gangrene. Diabetes mellitus is a major risk factor for lower extremity arterial occlusion, with infrapopliteal arteries most commonly affected. Patients with diabetic foot ulcers (DFUs) have a high prevalence of neurovascular complications, poor healing, and elevated amputation and mortality rates. Large-scale cohort studies indicate that five-year survival after amputation in this population is only about 50%, underscoring the need for more effective therapies.

Endovascular revascularization has become the first-line treatment for diabetic lower limb ischemia. However, despite successful revascularization, persistent microvascular dysfunction and difficult-to-heal ulcers remain common due to chronic inflammation, impaired angiogenesis, and tissue repair deficits. Current advanced wound dressings provide limited benefit and are often costly.

Read more

Cold atmospheric plasma (CAP) has emerged as a promising adjunctive therapy, with demonstrated antimicrobial activity-including efficacy against multidrug-resistant organisms-and the ability to promote microcirculation and wound healing. CAP generates reactive oxygen and nitrogen species that disrupt bacterial membranes and may also stimulate tissue regeneration. Preclinical and clinical studies suggest that CAP can accelerate healing in chronic wounds and is well tolerated by patients.

Given these advantages, the present study aims to assess the efficacy and safety of CAP combined with endovascular intervention in patients with diabetic foot ulcers and lower extremity arterial occlusion, to inform future clinical application of this novel technology.

Read the detailed description

End-stage peripheral arterial disease (PAD) is characterized by critical limb ischemia, which manifests clinically as insufficient arterial perfusion leading to ischemic rest pain, ulceration, and gangrene. A substantial proportion of these cases occur in patients with diabetes complicated by lower extremity arterial occlusion. Ischemia in diabetic patients predominantly affects infrapopliteal arteries, often presenting bilaterally and symmetrically, with diffuse lesions that commonly involve the entire vessel wall. These patients are more prone to both intimal atherosclerosis and medial arterial calcification.

A large multicenter cohort study in China that enrolled 669 patients with diabetic foot ulcers from 15 tertiary hospitals reported that more than 98% had underlying neurovascular pathology. The overall amputation rate was 19.03%, with major and minor amputation rates of 2.14% and 16.88%, respectively. Notably, the five-year survival rate after amputation was approximately 50%, which is lower than that observed for many malignancies. According to a large European cohort study, about half of diabetic foot ulcers are attributable to neuropathic or ischemic etiologies. Both macrovascular and microvascular dysfunctions jointly impair tissue perfusion and exacerbate diabetic foot pathology. From a clinical perspective, successful arterial revascularization alone is not sufficient; maintenance and optimization of distal microcirculatory perfusion following revascularization are also essential for effective ulcer healing.

With advances in endovascular techniques, infrapopliteal angioplasty has become the first-line treatment for diabetic lower limb ischemia, with proven efficacy. However, even after successful revascularization, some patients continue to suffer from inadequate distal perfusion due to microembolization or from persistent, hard-to-heal ulcers driven by the underlying pathophysiology of diabetic wounds. Several studies have demonstrated that diabetic patients experience metabolic dysregulation, local wound hyperglycemia, and accumulation of advanced glycation end-products (AGEs); combined with immune dysfunction and chronic inflammation, these factors maintain wounds in a persistent inflammatory state. Chronic inflammation suppresses vascular endothelial growth factor (VEGF) and angiopoietin-1 (ANG-1) expression, impairs endothelial cell function, and leads to angiogenesis disorders and delayed tissue repair. Reduced VEGF and ANG-1 expression has been confirmed in skin specimens from diabetic patients. In addition, peripheral neuropathy further inhibits neovascularization.

Despite widespread clinical use of advanced wound dressings-such as hydrogels, natural or synthetic polymer-based products, and other dressings designed specifically for diabetic ulcers-treatment efficacy remains limited, and costs can be substantial. For patients with diabetic foot ulcers complicated by large-vessel occlusion, ongoing assessment and support of distal microvascular perfusion remain a major unmet clinical need, even after successful revascularization.

Cold atmospheric plasma (CAP) has been widely adopted in medical applications and has demonstrated robust antimicrobial activity as well as the capacity to enhance tissue microcirculation and promote wound healing, with excellent patient tolerance. Multiple preclinical and clinical studies have confirmed the bactericidal efficacy of CAP, including activity against multidrug-resistant organisms. For example, Brun et al. reported that CAP effectively eradicates Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA) in vitro, achieving results comparable to antibiotics but with higher efficiency. Lis et al. found that CAP could also inactivate MRSA, Klebsiella pneumoniae, and Acinetobacter baumannii. Korean researchers Kim et al. demonstrated that CAP effectively disrupts biofilms formed by P. aeruginosa and other pathogens in canine skin and ear infections. In a prospective clinical study, Stratmann et al. showed that CAP treatment accelerates wound healing in diabetic foot ulcers. Boekema et al. [6] reported a significant reduction in bacterial load and no serious adverse events in patients with P. aeruginosa infections treated with CAP, confirming its safety profile.

The antimicrobial mechanism of CAP is primarily attributed to the generation of reactive oxygen and nitrogen species (RONS), which induce local free radical formation and disrupt microbial membranes, leading to apoptosis without fostering antimicrobial resistance. This highlights CAP as a valuable adjunct to conventional antibiotic therapy, especially for wounds infected with multidrug-resistant bacteria.

Importantly, CAP's benefits extend beyond antimicrobial effects. Numerous studies indicate that CAP promotes wound healing not only by eliminating pathogens but also by directly activating tissue regeneration. At the cellular level, CAP has been shown to modulate fibroblasts, vascular endothelial cells, and keratinocytes. Stratmann et al. observed that CAP enhanced tissue regeneration in diabetic foot ulcers without a corresponding decrease in colony-forming units, suggesting a regeneration mechanism independent of bactericidal action. In the study by Brehmer et al., CAP (PlasmaDerm device) significantly improved healing rates in lower extremity venous ulcers compared with standard care. These findings imply that CAP can accelerate tissue regeneration and shorten healing time, regardless of its antimicrobial effects.

Delayed wound healing is often accompanied by local microcirculatory disorders, resulting in decreased collagen production and impaired proliferation and migration of keratinocytes and fibroblasts. Several clinical trials have demonstrated that CAP exposure at therapeutic doses increases local skin blood flow and tissue oxygen saturation without raising skin temperature. The underlying mechanism may involve nitric oxide (NO) permeation, modulation of cysteine disulfide bonds and acidic lipid groups, reduced local pH, and improved microcirculation. In animal and cellular experiments, Arndt et al. demonstrated that CAP induces oxidative stress pathways in a paracrine and autocrine manner, stimulating keratinocytes, fibroblasts, and endothelial cells to produce vascular growth factors (EGF, FGF-2, IL-8, uPA, angiopoietin, VEGF), thereby promoting angiogenesis.

Based on these findings, this study aims to evaluate the efficacy and safety of CAP combined with endovascular intervention in patients with diabetic foot ulcers complicated by lower extremity arterial occlusion, providing essential evidence to support future large-scale clinical application of CAP.

Being tested
Cold atmospheric plasma (CAP), Sham Procedure, Successful infrapopliteal angioplasty
Keywords
cold atmospheric plasma, diabetic foot ulcers, lower extremity arterial occlusion
Medical subject headings
Diabetic Foot

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cold atmospheric plasma (CAP)Device

    CAP therapy will be administered once daily for the first five days and then every other day thereafter, for a total of 13 sessions. Each session will last approximately 25 minutes, as recommended by the manufacturer. During treatment, the affected limb will be enclosed in a sterile treatment bag, sealed with medical adhesive tape. The CAP device will operate in two sequential modes: a "disinfection mode" delivering ozone-rich (O₃) plasma-activated gas for 20 minutes, followed by a "healing mode" delivering nitric oxide (NO)-rich plasma-activated gas for 5 minutes. All procedures will be performed in accordance with the manufacturer's instructions and the device's standard operating protocol.

  • Sham ProcedureDevice

    Participants in the placebo group will undergo a sham procedure, in which the electric field required for plasma generation will be disabled, so that no plasma will be produced. Only the operating sounds of the device will be simulated, ensuring blinding for both participants and clinical staff.

  • Successful infrapopliteal angioplastyOther

    All patients will undergo successful infrapopliteal angioplasty, with less than 30% residual stenosis confirmed by digital subtraction angiography.

Study groups in NCT07073040
Study groupRoleWhat they receive
CAP therapyActive comparatorNot described
Receives: Device: Cold atmospheric plasma (CAP); Other: Successful infrapopliteal angioplasty
the placebo groupPlacebo comparatorNot described
Receives: Device: Sham Procedure; Other: Successful infrapopliteal angioplasty

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in ulcer area between groups

    The ulcer area (cm²) will be measured daily during the first five days, and every other day for the subsequent eight visits (13 follow-up assessments in total)

    Measured: From Baseline (Day 0) to Day 21 post-randomization

Secondary outcomes (9)
  1. Time to 10% reduction in ulcer area

    The time from randomization to the first occurrence of a 10% reduction in ulcer area

    Measured: From Baseline (Day 0) to Day 21 post-randomization

  2. Time to 20% reduction in ulcer area

    The time from randomization to the first occurrence of a 20% reduction in ulcer area.

    Measured: From Baseline (Day 0) to Day 21 post-randomization

  3. Time to onset of clinical signs of infection

    The time from randomization to the first documented clinical sign of wound infection.

    Measured: From Baseline (Day 0) to Day 21 post-randomization

  4. Change in pain score

    Change in pain score, assessed by the Visual Analogue Scale (VAS; 0 = no pain, 10 = worst imaginable pain; higher scores indicate greater pain severity)

    Measured: From Baseline (Day 0) to Day 21 post-randomization

  5. Change in quality of life (EQ-5D questionnaire)

    Measured: Baseline (Day 0) and Day 21 post-randomization

  6. Change in quality of life (SF-12 questionnaire)

    Measured: Baseline (Day 0) and Day 21 post-randomization

  7. Incidence of local skin irritation

    Measured: From Baseline (Day 0) to Day 21 post-randomization

  8. Incidence of local bleeding

    Measured: From Baseline (Day 0) to Day 21 post-randomization

  9. Incidence of local burning sensation

    Measured: From Baseline (Day 0) to Day 21 post-randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Jul 2025
  2. Study start22 Jul 2025
  3. Primary completion10 Apr 2026 (estimated)
  4. Study completion6 May 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
86 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07073040
Sponsor's protocol ID
PROSPECT
Acronym
PROSPECT
Status last verified
Dec 2025
First submitted
29 Jun 2025
Last updated
30 Jan 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Cold atmospheric plasma (CAP) and Successful infrapopliteal angioplasty in people with Diabetic Foot Ulcers (DFU) and Lower Extremity Arterial Occlusion, run by Shenyang Medical College at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Yun-En Liu, MD (86-24-62215130, lye9901@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in ulcer area between groups (time frame: From Baseline (Day 0) to Day 21 post-randomization). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jan 2026.

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