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Completed

NCT Number: NCT01305070

Standard Balloon Angioplasty Versus Angioplasty With a Paclitaxel-eluting Balloon for Femoral Artery In-stent Restenosis

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).

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Medical Care Center Prof. Mathey, Prof. Schofer

Hamburg, Free and Hanseatic City of Hamburg, 22527, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 21 years old.
  • Patient must sign informed consent form.
  • Patient must agree to participate in the study and comply with follow-up requirements.
  • Clinically, all patients must be in Rutherford category 2 to 4.

Angiographic Inclusion Criteria:

  • Planned angioplasty of in-stent restenoses (degree of stenosis 70-100%) within the SFA. The target lesion must not extend beyond the stent margins. In cases of two or more stenotic regions within the stented segment, these are considered separate lesions if there is a nonstenotic or only mildly stenotic (< 30%) segment of at least 2 cm in length between them. Otherwise, they are considered a single lesion. In case of separate lesions, only the proximal lesion will be taken as the target lesion!
  • The length of the in-stent lesion should be at least 1 cm and maximally 20 cm (measurement by radiopaque ruler).
  • The degree of target lesion stenosis must be determined by pre-interventional duplex ultrasound.
  • The target lesion region starts at the origin of the SFA and ends distally at the femoropopliteal crossover (crossing by SFA of medial rim of femur in the PA projection).
  • Patency (< 50% stenosis) of popliteal artery and at least 1 infragenicular artery.

Exclusion criteria

General:

  • Patient is currently participating in another clinical trial.
  • Pregnancy or pregnancy planned during study duration.
  • Life expectancy less than 1 year.
  • Co-morbidities preventing study participation.
  • Severe coagulation disorders.
  • Current treatment with anticoagulants other than aspirin, ticlopidine, clopidogrel or prasugrel.
  • Active gastric ulcer or gastrointestinal bleeding.
  • Thrombotic occlusion of the target vessel within previous 4 weeks.
  • Treatment of target lesion with laser or atherectomy devices.
  • Dialysis dependency.
  • Manifest hyperthyreosis.
  • Known allergy against contrast agent that cannot be adequately controlled by usual premedication.
  • Known heparin intolerance.
  • Known paclitaxel intolerance.

Angiographic:

  • Target lesion extends into the popliteal artery.
  • Symptomatic untreated inflow lesion > 50% in ipsilateral iliac arteries. Pretreatment of iliac stenoses is possible.
  • SFA lesions > 50% stenosis proximal and/or distal to the target lesion that require treatment.
  • Target lesion extends beyond the stent margins.

Treatment and study plan

Admiral Xtreme

Device

For balloon angioplasty of in-stent restenosis in the superficial femoral artery

Other names: Admiral Xtreme, Invatec

In.Pact Admiral

Device

For balloon angioplasty of in-stent restenosis in the superficial femoral artery

Other names: In.Pact Admiral, Invatec

Primary outcomes

  1. Duplex-ultrasound determined recurrent restenosis in the superficial femoral artery (SFA)

    Time frame: 6 month

    Binary restenosis rate by Duplex-ultrasound >= 50% measured as proximal peak velocity ratio PVR[prox] >= 2.4

Secondary outcomes

  1. Recurrent restenosis within the stent at 12 month

    Time frame: 12 month

    Recurrent restenosis >= 50% measured as proximal peak velocity ratio PVR[prox] >= 2.4

  2. Clinically driven target lesion revascularization (TLR) at 6 and 12 month

    Time frame: 6 and 12 month

  3. Recurrent stenosis >= 70% within the stent at 6 and 12 month

    Time frame: 6 and 12 month

    Recurrent restenosis >= 70% measured as proximal peak velocity ratio PVR[prox] >= 3.4

  4. Clinical and hemodynamic parameters

    Time frame: at 1, 6 and 12 month

    Walking distance, ABI, Rutherford category

  5. Primary angiographic success rate

    Time frame: 12 month

    Angiographic sucess: <50% residual stenosis

  6. Major adverse vascular events (MAVE)

    Time frame: 12 month

  7. Death

    Time frame: 12 month

  8. Impact of "bail-out" stent-in-stent placement on 6-and 12-month end points

    Time frame: 6 and 12 month

Sponsors and collaborators

Lead sponsor

Medical Care Center Prof. Mathey, Prof. Schofer, Ltd.

Other

Registry information

Official study title

Femoral Artery In-Stent Restenosis (FAIR) Trial

Acronym: FAIR

Important dates

Study start
2010
Primary completion
2012
Study completion
2013
First posted
Feb 28, 2011
Registry last updated
Feb 6, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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