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Clinical Trial Summary

To evaluate the preliminary efficacy of combination of cutting and drug-coated balloon for the treatment of resistant AVF stenosis.


Clinical Trial Description

This is a single arm pilot study recruiting 19 participants with resistant AVF stenosis (defined as having > 30% residual stenosis after optimal balloon angioplasty) to receive cutting and drug-coated balloon. The outcome measure is target lesion primary patency at 6 months. Outcome will be clinically driven. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05961852
Study type Interventional
Source Singapore General Hospital
Contact
Status Completed
Phase Phase 1
Start date August 15, 2018
Completion date June 30, 2019

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