Medical Care Center Prof. Mathey, Prof. Schofer
Hamburg, Free and Hanseatic City of Hamburg, 22527, Germany
NCT Number: NCT01305070
Comparison of recurrent-restenosis rates 6 months after angioplasty of in-stent restenoses or in-stent reocclusions in the superficial femoral artery (SFA) using either a standard balloon (Admiral Xtreme, Invatec) or a paclitaxel-eluting balloon (In.Pact™ Admiral, Invatec).
Looking for future studies?
Notify Me21 year and older
All sexes
Interventional
Phase 4
Hamburg, Free and Hanseatic City of Hamburg, 22527, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Angiographic Inclusion Criteria:
Exclusion criteria
General:
Angiographic:
For balloon angioplasty of in-stent restenosis in the superficial femoral artery
Other names: Admiral Xtreme, Invatec
For balloon angioplasty of in-stent restenosis in the superficial femoral artery
Other names: In.Pact Admiral, Invatec
Time frame: 6 month
Binary restenosis rate by Duplex-ultrasound >= 50% measured as proximal peak velocity ratio PVR[prox] >= 2.4
Time frame: 12 month
Recurrent restenosis >= 50% measured as proximal peak velocity ratio PVR[prox] >= 2.4
Time frame: 6 and 12 month
Time frame: 6 and 12 month
Recurrent restenosis >= 70% measured as proximal peak velocity ratio PVR[prox] >= 3.4
Time frame: at 1, 6 and 12 month
Walking distance, ABI, Rutherford category
Time frame: 12 month
Angiographic sucess: <50% residual stenosis
Time frame: 12 month
Time frame: 12 month
Time frame: 6 and 12 month
Medical Care Center Prof. Mathey, Prof. Schofer, Ltd.
Other
Femoral Artery In-Stent Restenosis (FAIR) Trial
Acronym: FAIR
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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