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 volunteersQualifiers
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
Parallel
Treatments tested in this trial
Percutaneous transluminal angioplasty
Procedure/SurgeryPercutaneous transluminal angioplasty of the leg
Treatment groups
Trial outcomes
Primary outcomes
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.
Secondary outcomes
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.
Other outcomes
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.
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).
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Heinrich-Heine University, Duesseldorf
Lead sponsor
German Diabetes Center
Collaborator