Evaluation of morphologic differences of instent restenosis after femoropopliteal stent angioplasty with different stent designs

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00028852

Enrollment

400

Registered

2022-04-25

Start date

2022-04-13

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I70.20

Interventions

Group 1: stentangioplasty SMART Control Stent Group 2: stentangioplasty Supera Peripheral Stent Group 3: stentangioplasty GORE® VIABAHN® Endoprothese Group 4: stentangioplasty BioMimics 3D Stent G

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Instent restenosis femoropopliteal

Exclusion criteria

Exclusion criteria: No Instent restenosis femoropopliteal

Design outcomes

Primary

Measure	Time frame
Localization and extent of stenosis within the stent.	—

Secondary

Measure	Time frame
Frequency of stent occlusion Time from implantation to restenosis/reintervention Predictors for re-stenosis/stent occlusion Clinical severity stage at the time of reintervention	—

Countries

Germany

Contacts

Public ContactTanja Böhme

Universitäts-Herzzentrum Bad Krozingen

Tanja.Boehme@universitaets-herzzentrum.de004976334020

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026