Clinical Trials Logo

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

See also
  Status Clinical Trial Phase
Active, not recruiting NCT06056206 - The SIR-POBA Shunt Trial N/A
Completed NCT05034939 - FLEX Vessel Prep Prior to Angioplasty in Native Arteriovenous Fistulae (AVF) N/A
Active, not recruiting NCT05545267 - Monitoring of Dialysis Vascular Accesses During Angioplasty Under Echodoppler
Recruiting NCT04543539 - IN.PACTâ„¢ AV Access Post-Approval Study (PAS002)
Completed NCT04070365 - FLEX Arteriovenous Access Registry
Completed NCT03366727 - AcoArt III / Arterio-venous Fistula in China N/A
Completed NCT03213756 - Isometric Preoperative Exercise on Autologous Arteriovenous Fistulas. Randomized Clinical Trial N/A
Completed NCT04312711 - 3D Time-of-Flight Magnetic Resonance Angiography in Hemodialysis Patients With Arteriovenous Fistula N/A
Completed NCT03041467 - IN.PACTâ„¢ AV Access IDE Study N/A