An observational study in Iliac Artery Disease, sponsored by Assiut University. Not yet recruiting. Per ClinicalTrials.gov, last updated 2025-06-10.
Sponsored by Assiut University · Observational
To evaluate the safety, efficacy, and outcomes of endovascular strategies for protection of the contralateral CIA in patients with symptomatic unilateral CIA occlusive disease
Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.
Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Patients attending the Vascular Surgery Clinics in Assiut University Hospitals complaining of unilateral CIA ostial occlusive disease, Rutherford category 3, 4and 5 will be recruited to participate in the study.
with or without combined iliac or femoropopliteal or infrapopliteal lesions.
Asymptomatic Contralateral limb.
Patent at least one run-off vessel
Exclusion Criteria:
contralateral CIA occlusion
Previous endovascular or surgical procedures for the same lesion
Hypersensitivity to contrast material
Presence of aortic or iliac aneurysms
Patients with unsalvageable limb
Non atherosclerotic lesions
Stenting of common iliac artery by balloon mounted stent
Primary patency of both common iliac arteries
Time frame: 2 years
No study locations are listed for this record.
Plan to share: No
This study is not yet recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.
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Assiut University