Completed PHASE4 INTERVENTIONAL 2-arm NCT00309595

The Study to Compare SMART Nitinol Stent and Balloon Angioplasty (SIT-UP)

A Multi-Center Prospective, Randomized, Two-Arm Clinical Investigation of the Cordis SMARTTM Nitinol Self Expandable Stent Versus Balloon Angioplasty Only for the Treatment of Superficial Femoral Artery Occlusions.

Sponsor: Cordis US Corp.

Conditions Superficial Femoral Artery Occlusions

Interventions balloon stent

Updated 7 times since 2017 Last updated: Jun 10, 2009 Started: Dec 31, 2005 Primary completion: May 31, 2009 Completion: May 31, 2009

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE4 clinical study on Superficial Femoral Artery Occlusions, this trial is completed. The trial is conducted by Cordis US Corp. and has accumulated 7 data snapshots since 2005. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

7 versions recorded

Dec 2025 — Present [monthly]

Completed PHASE4
Sep 2024 — Dec 2025 [monthly]

Completed PHASE4
Jul 2024 — Sep 2024 [monthly]

Completed PHASE4
Jan 2021 — Jul 2024 [monthly]

Completed PHASE4
Jun 2018 — Jan 2021 [monthly]

Completed PHASE4

▶ Show 2 earlier versions

Feb 2017 — Jun 2018 [monthly]

Completed PHASE4
Jan 2017 — Feb 2017 [monthly]

Completed PHASE4

First recorded

Dec 2005

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Cordis US Corp.

Data source: Cordis US Corp.

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Bern, Switzerland
• Zurich, Switzerland