Early Percutaneous Transluminal Angioplasty in Diabetic Foot Syndrome (PTA-DFS)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHeinrich-Heine University, Duesseldorf

About this trial

The planned study is a Randomized Controlled Monocentric Trial, which will provide evidence on whether early angiography in percutaneous transluminal angioplasty (PTA) readiness ("immediate" treatment, within 48h) has advantages over the "standard of care", i.e., an elective procedure ("elective PTA") for the treatment of diabetic foot ulcer (DFU). The primary study endpoint is to investigate the impact of the "early PTA" within 48 hours on wound-healing assessed by wound area changes after PTA using a 3D-camera with artificial intelligence (AI)-based wound-analysis-system. The secondary endpoint is the effect of early PTA on the combined occurrence of major adverse limb (MALE) and cardiac events (MACE) over 12 months post-angioplasty using time-to-event analysis. Data will be collected at baseline, 24 hours, 1, 2, 3, 6, and 12 months after PTA. Diabetic kidney disease, distal symmetric polyneuropathy, retinopathy, cardiomyopathy, laboratory analyses, clinical scores, AI-based fundus photography, echocardiography, duplex sonography, and pulse oscillography will be assessed. Explanatory variables for wound healing are wound microbiome changes using whole-genome sequencing and oxygen saturation of the wound environment measured using near-infrared spectroscopy. Altered microbiome composition in ulcers can lead to severe local and systemic infections and complications, including major amputations. Nevertheless, the specific significance of the wound microbiome composition in chronic ischaemic ulcers in type 2 diabetes and the impact of PTA on the wound microbiome in type 2 diabetes is unclear. The exact timing for treating peripheral arterial disease (PAD) by revascularization in DFU after initial diagnosis is unknown and has yet to be fully understood.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

volunteer adults

written informed consent

HbA1c < 10%

PAD Stage After Fontaine IV (foot ulcer)

Disqualifiers

Acute leg ischemia (sudden onset, sensorimotor deficits, pale extremity, pain, loss of pulse, and shock).

Type 1 diabetes mellitus (GADA, ICA, IA-2A, ZnT8A positive).

Minors or subjects incapable of giving consent

Pregnant or breastfeeding women

Trial design

Design model

Parallel

Treatments tested in this trial

  • Percutaneous transluminal angioplasty

    Procedure/Surgery

    Percutaneous transluminal angioplasty of the leg

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: PTA within 48hExperimental treatment 0 interventions
Group B: PTA within 6 weeksActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Effect of PTA within 48h on changes of the wound area

Assessment of the impact of 'early' PTA (performed within 48 hours) on wound healing, evaluated through changes in wound area using a 3D camera with an AI-based wound analysis system over a 12-month follow-up period.

Time frame
Wound area difference from baseline to last visit

Secondary outcomes

1

Effect of PTA within 48h on the cummulative occurrence of MALE and MACE

Assessment of major adverse limb (MALE) and cardiac events (MACE) post-angioplasty using time-to-event analysis.

Time frame
Baseline to one year follow up

Other outcomes

1

Effect of PTA within 48h on changes in wound microbiome

Exploratory variable for the primary endpoint: Shift in bacterial taxa with different oxygen requirements (aerobes, anaerobes). Analysed using appropriate statistical methods, such as Generalized Linear Mixed Models (GLMMs), accounting for treatment group ('immediate' PTA vs. 'elective' PTA), bacterial taxa, and time, with random effects to adjust for individual variability.

Time frame
Baseline to one year follow-up
2

Effect of PTA within 48h on changes in oxygen saturation of wound environment

Exploratory variable for the primary endpoint: Change in oxygen saturation in the wound environment, measured by multispectral near-infrared spectroscopy (NIRS).

Time frame
Baseline to one year follow up

Sponsors and contacts

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Heinrich-Heine University, Duesseldorf

Lead sponsor

German Diabetes Center

Collaborator