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Nowadays, stenting is became a standard of care in revascularization for superficial femoral artery (SFA) atherosclerotic lesions. However, the Achilles' heel of this technique remains in-stent restenosis (ISR). While most of local therapies have failed to demonstrate significant benefit, studies for the treatment of SFA ISR are lacking and percutaneous transluminal angioplasty remains the current standard of care for this indication. Recent studies have shown successful results of drug eluting balloon in the treatment of SFA de-novo lesions and of coronary ISR. FREERIDE, a French prospective cohort has been set up to evaluate the safety and the efficacy of drug eluting balloon (DEB) for the treatment of SFA atherosclerotic lesions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| drug eluting balloon | In this observationnal study, the intervention of interest is the use of drug eluting balloon in stent restenosis. Only the treated patients were included in this cohort. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PacLitaxel Eluting Balloon Application | Procedure | Stenting is a standard of care in revascularization for superficial femoral artery (SFA) atherosclerotic lesions. However, the Achilles' heel of this technique remains in-stent restenosis (ISR). While most of local therapies have failed to demonstrate significant benefit, studies for the treatment of SFA ISR are lacking and percutaneous transluminal angioplasty remains the current standard of care for this indication. Recent studies have shown successful results of drug eluting balloon in the treatment of SFA de-novo lesions and of coronary ISR. |
| Measure | Description | Time Frame |
|---|---|---|
| Target Lesion Revascularization (TLR) | at 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Major Adverse Events through | at 1 year | |
| Target extremity revascularization (TER) | at 1, 3, 6, 9, 12 and 18 months after surgery | |
| clinical improvement equal or above to a stage according to Rutherford classification without superficial femoral artery revascularization |
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Inclusion Criteria:
Exclusion Criteria:
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From December 2011 to December 2012 at 13 hospitals in France, we will include patients with symptomatic atherosclerotic lesions related to superficial femoral artery in-stent restenosis to undergo endovascular repair by paclitaxel drug eluting balloon. 100 patients will be included.
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| Name | Affiliation | Role |
|---|---|---|
| Thierry Reix, PU-PH | Amiens's Univeristy Hospital | Principal Investigator |
| Eric Ducasse, PU-PH | Pellegrin's University Hospital | Principal Investigator |
| Patrick Lermusiaux, PU-PH | Lyon's University Hospital | Principal Investigator |
| Jean-Marc Pernes, Practitioner | Antony's private Hospital | Principal Investigator |
| Nicolas Louis, PH | Le Raincy-Montfermeuil Hospital | Principal Investigator |
| Antoine Sauget, Practitioner | Pasteur's private Hospital | Principal Investigator |
| Philippe Commeau, Practitioner | Ollioules private Hospital | Principal Investigator |
| Jean-Noel Albertini, PU-PH | St Etienne University Hospital | Principal Investigator |
| Olivier Planché, PH | Le Plessis-Robinson private hospital (CMC) | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nantes University Hospital | Nantes | 44093 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27890526 | Derived | Bague N, Julia P, Sauguet A, Pernes JM, Chatelard P, Garbe JF, Penillon S, Cardon JM, Commeau P, Planche O, Guyomarch B, Goueffic Y. Femoropopliteal In-stent Restenosis Repair: Midterm Outcomes After Paclitaxel Eluting Balloon Use (PLAISIR Trial). Eur J Vasc Endovasc Surg. 2017 Jan;53(1):106-113. doi: 10.1016/j.ejvs.2016.10.002. Epub 2016 Nov 24. |
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| ID | Term |
|---|---|
| D058729 | Peripheral Arterial Disease |
| ID | Term |
|---|---|
| D050197 | Atherosclerosis |
| D001161 | Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |
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|
to assess primary maintenance of clinical improvement |
| at 1, 3, 6, 9, 12 and 18 months |
| peak systolic velocity index without Target Lesion Revascularization | to assess primary patency | at 1, 3, 6, 9, 12 and 18 months |
| Quality of life assessment by EQ5D questionnaire | at 1, 3, 6, 9, 12 and 18 mois after surgery |
| post-angioplasty restenosis | at 1, 3, 6, 9, 12 and18 months after surgery |
| drug relief success without balloon break | during surgery |
| Length of hospitalization stay | at 1 year |
| clinical improvement equal or above to a stage according to Rutherford classification with possible superficial femoral artery surgery | to assess secondary maintenance of clinical improvement | at 1, 3, 6, 9, 12 and 18 months |
| peak systolic velocity index | to assess secondary patency | at 1 year |
| intra-stent restenosis | significant whether restenosis >50% and peak systolic velocity index > 2.4 | at 1, 3, 6, 9, 12 and 18 months after surgery |
| Max Amor, PH | Essey-les-Nancy Private hospital (Polyclinique Pasteur) | Principal Investigator |
| Jean-Marie Cardon, Dr | Nimes private Hospital (clinique des fransiscaines) | Principal Investigator |
| Alain Cardon, PH | Rennes's University Hospital | Principal Investigator |
| D002318 |
| Cardiovascular Diseases |
| D016491 | Peripheral Vascular Diseases |