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Clinical Trials in Germany / NCT06124586
Recruiting Not applicable

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

NCT06124586 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2024-02-01
Last updated
2026-02-04

Condition(s) studied

Diabetic FootDiabetes MellitusPeripheral Arterial DiseaseDiabetic NeuropathiesDiabetic RetinopathyAnemiaUlcer FootUlcer IschemicDiabetic Polyneuropathy

Investigational drug(s) / intervention(s)

Percutaneous transluminal angioplasty

Percutaneous transluminal angioplasty: Percutaneous transluminal angioplasty of the leg

Study summary

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * volunteer adults * written informed consent * presence of known manifest T2D and fulfilment of the following criteria: * HbA1c \< 10% * presence of pAVD with fulfillment of the following criteria: * PAD Stage After Fontaine IV (foot ulcer) * Presence of foot ulcer with fulfillment of the following criteria: * Foot ulceration without indication for emergency surgical care from stage Wagner 1. * Age \>18 years Exclusion Criteria: * 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 * Treatment with certain drugs (immunosuppressive therapy, * Immunomodulators, chemotherapy, antibiotic therapy \< 2 weeks before * intervention) * Diseases of the pancreas * Severe neurological or psychiatric disease * Known presence of malignant tumor disease within the past 5 years * Participation in other interventional trials and receipt of investigational medication within the last 30 days * Blood or plasma donation within the last 3 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University-Hospital Düsseldorf Division of Cardiology, Pulmonary Disease and Vascular Medicine Düsseldorf Germany Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06124586 on ClinicalTrials.gov ↗ ← All trials in Germany