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Clinical Trial Summary

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

- A total of 100 subjects with isolated popliteal artery lesions according to inclusion and exclusion criteria will be enrolled.

- All popliteal artery lesions will be treated with drug-eluting balloon (In.PACT Admiral, Medtronic). • Atherectomy or use of bare nitinol stent in combination with drug-eluting balloon is allowed • Patients will be followed clinically for 12 months after the procedure.

- Imaging study (Duplex ultrasound, CT angiography or catheter angiography) follow-up will be performed at 12 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02698345
Study type Observational
Source Yonsei University
Contact
Status Recruiting
Phase
Start date January 2016
Completion date March 2021

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04546477 - Prospective Multicenter Study to Confirm the Performance of the Renzan Stent in Treatment of SFA/POP Artery Disease N/A