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Analysis of the Different Strategies for Revascularization of the Lower Limbs by Peripheral Angioplasty

R

Ramsay Générale de Santé

Status

Unknown

Conditions

Angioplasty
Peripheral Arterial Disease

Treatments

Other: One or two phone call

Study type

Observational

Funder types

Other

Identifiers

NCT05155462
2018-A00868-47

Details and patient eligibility

About

Peripheral arterial disease (PAD) caused by atherosclerosis causes damage to the arteries originating in the aorta (descending) from the iliacs to the extremities of the lower limbs. It causes significant morbidity and mortality. Percutaneous revascularization plays a key role in the management of these patients. Many percutaneous treatment options have been developed: arteriectomy, naked stents, active balloons and active stents. Of these, only paclitaxel-active stents were successful in reducing the rates of restenosis and reoperation in patients with superficial femoral artery injury.The main objective is to study symptomatic improvement at 1 year of patients treated with revascularization of the lower limbs.

Enrollment

330 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient treated by the peripheral angioplasty department of Claude Galien Hospital from January 2010 and with at least 1 year of follow-up after the revascularization procedure
  • Patient treated for symptomatic chronic ischemia of the lower limbs defined by Rutherford categories 2-4 and / or Leriche stage greater than 2a
  • Stenosis or restenosis (history of balloon angioplasty, active balloon or bare stent)
  • Degree of stenosis ≥ 50% by angiographic evaluation visual, by CT scan or by Doppler ultrasound
  • Patient affiliated or beneficiary of a social security scheme
  • Patient aged 18 or over
  • Patient having been informed and not opposing this research

Exclusion criteria

  • Medical history of myocardial infarction or stroke within 3 months of the revascularization procedure
  • Unstable angina at the time of the revascularization procedure
  • Sepsis at the time of the revascularization procedure
  • Major under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
  • Hospitalized without consent
  • Pregnant, breastfeeding or parturient woman

Trial design

330 participants in 1 patient group

Patient treated for defined symptomatic chronic lower extremity ischemia
Treatment:
Other: One or two phone call

Trial contacts and locations

1

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Central trial contact

Jean-François Oudet; Marie-Hélène Barba

Data sourced from clinicaltrials.gov

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