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Not yet recruiting NCT07014072

Comprehensive Limb Evaluation and Arterial Revascularization With Toe Pressure Optimization Registry

No phase Interventional Critical Limb Ischemia (CLI)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: intensive toe pressure evaluation, data collection.
Who it may be relevant to
Registry conditions: Critical Limb Ischemia (CLI). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

To address the heterogeneity of practices, better understand the outcomes of cricital limb theatening ischemia (CLTI) patients after endovascular interventions, and recognize effective endovascular options for infrapopliteal artery revascularization in CLTI, our prospective registry aims to tackle the critical question of whether intensive toe pressure evaluation, guiding repeat revascularization using predetermined thresholds (\<30 mmHg or decrease \>10% from immediate postoperative assessment), could optimize outcomes in patients with CLTI.

Detailed description

Cricital limb theatening ischemia (CLTI) represents the most advanced stage of peripheral arterial disease (PAD), leading to high mortality rates and limb loss. A primary endovascular strategy is now preferred for most patients with CLTI who have occlusive disease of the tibial arteries. This is especially true for the elderly, diabetic patients, and those without suitable venous conduits for bypass. Patients with CLTI and infra-popliteal occlusive disease do not always respond well to the provided treatment, but the underlying reasons, particularly in those showing good initial results after endovascular revascularization, remain to be determined.

The literature strongly supports the use of drug-eluting stents (DES) in treating infrapopliteal arteries. DES are associated with significant improvements in patency, reduced rates of restenosis and reintervention, and better Rutherford-Becker classification and healing of trophic disorders. However, contrary to initial expectations, the SAVAL trial, whose data were made public in December 2023, comparing a DES dedicated to infra-popliteal arteries with percutaneous transluminal angioplasty in patients with CLTI, failed to meet its primary efficacy (increased primary patency and reduced major adverse events rate) and safety objectives at 12 months, despite preliminary data suggesting an advantage in using DES for treating short lesions. A possible explanation is the significant heterogeneity of practices, with less than half of the patients receiving optimal medical treatment and intensive follow-up, highlighting the need for a comprehensive review of treatment strategies in this challenging patient population.

The lack of an established objective follow-up protocol for this patient group underscores the need for innovative approaches. Currently, there is no widely available consensus indicator to estimate whether the revascularization provided will be sufficient to prevent amputation. The Delta-Perf study has completed its recruitment and is expected to provide results on foot perfusion analysis in patients with CLTI before and after revascularization and its predictive value on amputation-free survival. However, despite high initial technical success rates for endovascular interventions, early failure of these minimally invasive procedures is common.

Current recommendations support duplex scan monitoring and prophylactic reintervention for asymptomatic graft stenosis to promote long-term patency, but monitoring and reintervention strategies after endovascular management have been left to the practitioner's discretion. There are no ongoing studies to determine if the initial improvement observed in the foot is actually maintained, and there is little evidence to support indications for repeated interventions in CLTI. Clinical follow-up alone may be insufficient to detect restenosis, as patients may remain asymptomatic until the target artery is occluded, similar to venous grafts in bypasses. Likewise, measuring the ankle-brachial index (ABI) alone has limited value, given the difficulty in determining the level of restenosis, technical limitations in diabetic patients with calcified vessels, and variability in correlation with the severity of lesions.

It is likely that there are subgroups of patients who could benefit more than others from early reintervention. Toe pressure, in this context, offers a measurable, non-invasive, and clinically relevant parameter that can be consistently evaluated even in challenging cases, particularly in heavily calcified patients.

Interventions

  • Procedure intensive toe pressure evaluation
    This measurement is non-invasive, painless and is also carried out as part of the care in the follow-up of critical limb ischemia. It takes place like a blood pressure measurement except that it is carried out at the level of a toe.
  • Other data collection
    retrospective data

Primary outcome measures

  • Toe pressure with Systolic pressure measurement device [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]
Secondary outcome measures (6)
  • Evaluation of Survival [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]
  • Evaluation of the absence of target lesion occlusion. [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]
  • Evaluation of target lesion revascularization [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]
  • Evaluation of major adverse limb events [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]
  • Evaluation ofthe Wound healing with WiFi classification [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]
  • Evaluation of the Wound healing with colorimetry scale [Time frame: Day 15, Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years
  • Rutherford category 4 or 5
  • Wounds limited to toes or forefoot with a salvageable limb
  • Infrapopliteal lesions (infra-popliteal arteries) with >70% stenosis upon visual assessment during initial angiography

Exclusion criteria

  • Previous or planned major amputation of the target limb
  • Untreated aortoiliac/femoropopliteal stenotic disease limiting flow
  • History of infrapopliteal bypass on the target limb
  • Failure of percutaneous transluminal angioplasty of the target limb (technical failure)
  • Absence of angiographic evidence of a patent artery below the ankle ("desert foot")
  • Lesions located inside or near an arterial aneurysm
  • Life expectancy < 1 year
  • Acute limb ischemia
  • Septicemia or bacteremia

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Diagnostic

Study locations

France · 1 center
  • Centre Hospitalier Universitaire de Bordeaux — Bordeaux

Identifiers

NCT: NCT07014072 · CHUBX 2025/006 · 2025-A00272-47

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗