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Clinical Trial Summary

Comparing the result of of iliac vein stenting and compression therapy in management of recurrent venous ulceration.


Clinical Trial Description

Venous ulceration is the most common etiology of lower extremity ulceration, approximately affecting almost 1% of the world's population. although its overall prevalence is relatively low, the refractory nature of venous ulceration increases morbidity, mortality , the patient's quality of life, and have a significant financial burden on the global budget. the primary risk factors are: old age, obesity deep venous thrombosis, phlebitis and previous leg injuries. Iliac vein compression is a prevalent finding in patients with venous system pathology. It has a variety of causes, including May-Turner syndrome, endometriosis, bladder distension, common iliac artery aneurysm or internal iliac artery aneurysm. venous compression becomes clinically significant when there's an increase in venous pressure, which in turn causes venous insufficiency. This contributes to the development of a state of chronic venous stasis, which sequentially causes pooling of blood, triggers further capillary damage and activates inflammatory mediators with the end result of venous ulcer development and impaired wound healing. Located on bony prominences, venous ulcers are typically shallow, irregular with granulation tissue and fibrin present in their bases. A careful physical examination is required for a proper diagnosis, but he clinical challenge remains in its management, which includes prevention or the treatment of the clinical implications. Treatment modalities should always be directed to the cause of the ulcer; they can be divided into: - non invasive management, such as medical therapy, bandaging and dressings. - invasive, such as endovascular and surgical techniques. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04834232
Study type Observational
Source Assiut University
Contact
Status Enrolling by invitation
Phase
Start date May 1, 2021
Completion date December 1, 2021