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Clinical Trial Summary

- Prospective, single-arm, multi-center registry study

- A total of 150 subjects with iliac artery disease who meet all inclusion and exclusion criteria will be included.

- Patients will be followed clinically for 12 months after the procedure.

- Duplex ultrasound, CT or catheter-based angiography follow-up according to participating hospital's protocol will be performed at 12 months.

- Presence of stent fracture will be evaluated by plain radiography or fluoroscopy at 12 months.

- Quality of life by standardized questionnaires (at baseline & at 1 & 12 months)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02698358
Study type Observational
Source Yonsei University
Contact
Status Active, not recruiting
Phase
Start date December 2015
Completion date January 2021

See also
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