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Recruiting Not applicable

Revascularization of Single Vesrus Multiple Infrapopliteal Vessels in Chronic Limb Threatening Ischemia

NCT07068789 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-06-25
Last updated
2025-07-16

Condition(s) studied

Chronic Limb Threatening IschemiaInfrapopliteal Arterial Occlusive Disease

Investigational drug(s) / intervention(s)

balloon angioplasty

balloon angioplasty: endovascular angioplasty of infrapopliteal arteries performed using standard balloon catheters under fluroscopic guidance to restore blood flow to the ischemic area

Study summary

This interventional prospective study aims to assess the effectiveness of single vessel versus multiple vessel infrapopliteal angioplasty in patients with chronic threatening limb ischemia . The study compares limb salvage rates and clinical outcomes across two groups over a defined follow up period

Eligibility

Sex
ALL
Min age
40 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. patients aged 40 years or older 2. patients with Rutherford category "4" and "5" 3. patients with angiographic evidence of infrapopliteal vessel occlusive disease - Exclusion Criteria: 1. patients who refuse to participate in the study 2. patients with isolated proximal arterial disease (e.g SFA or popliteal ) without infrapopliteal involvement 3. patients who develop acute thrombosis , flow limiting dissection or perforation in the infrapopliteal arteries during intervention -

Primary outcome measure(s)

  • limb salvage rate — 6 months ( with optional follow up at 12 months )
    percentage of patients who remain free from major lower limb amputation during the period of follow up after angioplasty
  • limb salvage rate — 6 months ( with optional follow up at 12 months )
    percentage of patients who avoid major amputation during the period of follow up following angioplasty procedure

Trial sites (1)

FacilityCityRegionStatus
Faculty of Medicine of Sohag Sohag Sohag Governorate Recruiting
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 NCT07068789 on ClinicalTrials.gov ↗ ← All trials in Egypt