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NCT Number: NCT03622203

Outcome of CHAllenging lesioNs and Patients Treated With Polymer Free Drug-CoatEd Stent

Length of DAT (Dual Antiplatelet therapy) represents one of the most challenging choices for interventional cardiologist.

Prolonged DAT reduces risk of subsequent MI (Myocardial Infarction) with an increase in major bleedings, consequently with a neutral effect on survival [1].

Recently a Polymer-free Drug-Coated coronary stent has been tested in a randomized controlled trial with only one month of DAT due to its peculiar features, with an increased efficacy compared to BMS (Bare Metal Stent) and with a not negligible risk of ST at one year (about 2%)[2,3].

The RCT despite its promising design (inclusion of high risk patients like those with previous bleeding or with severe renal disease) showed a major limitation, that is:

1. patients who are often offered a Biofreedom in real life, that is those with active cancer or needing major surgery or on OAT (Oral Anticoagulation) 2. and patients with bifurcation and multivessel disease, that is those with an increased risk of ST [4] 3. STEMI patients [5] were underrepresented (less than 30%). Consequently we performed this multicenter study to evaluate safety and efficacy of Biofreedom in real life patients.

POCE (a composite end point of death, myocardial infarction, target lesion revascularization) and DOCE (cardiac death, MI-TLR and TLR) will be the primary end points, while its single components will be the secondary ones along stent thrombosis and with bleedings (Barc classification).

At least 12 months The Leaders FREE (2) reported an incidence of MACE of 9.4% at one year in overall patients. If there is a true difference in favour of the experimental treatment of 1.2%, then 870 patients are required to be 80% sure that the upper limit of a one-sided 95% confidence interval (or equivalently a 90% two-sided confidence interval) will exclude a difference when compared to non selected patients of more than 2% [5]

All patients implanting Biofreedom with these prespecified analysis:

1. Clinical

* Diabetic patients (both insulin and not insulin depenent) * Requiring oral anticoagulation * On active cancer (that is requiring chemio or radio-therapy and or surgery) * Requiring surgery * STEMI 2. Interventional

* Bifurcation (both provisional both 2 stents) * Multivessel * Ostial

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Key information

About this study

Our interest is to test the performance of these stents in real life patients

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Clinical
  • Diabetic patients (both insulin and not insulin depenent)
  • Requiring oral anticoagulation
  • On active cancer (that is requiring chemio or radio-therapy and or surgery)
  • Requiring surgery
  • STEMI
  • Interventional
  • Bifurcation (both provisional both 2 stents)
  • Multivessel
  • Ostial

Exclusion

  • clinical less than 18 years old or more than 80
  • interventional last remaing vessel

Treatment and study plan

Biofreedom

Device

Use of Biofreedom in real life patients

Primary outcomes

  1. Incidence of POCE (primary patient-oriented endpoint)

    Time frame: At least 6 months

    Incidence of POCE (a composite and mutual exclusive end point of death, myocardial infarction, target lesion revascularization)

Secondary outcomes

  1. Incidence of Death

    Time frame: At least 6 months

    Incidence of Death

  2. Incidence of Myocardial Infarction

    Time frame: At least 6 months

    Incidence of Myocardial Infarction

  3. Incidence of TLR

    Time frame: At least 6 months

    Incidence of target lesion revascularization

  4. Incidence of Cardiac Death

    Time frame: At least 6 months

    Incidence of Cardiac Death

  5. Incidence of MI-TLR

    Time frame: At least 6 months

    Incidence of Myocardia Infarction TLR

Sponsors and collaborators

Lead sponsor

A.O.U. Città della Salute e della Scienza

Other

Registry information

Official study title

Outcome of CHAllenging lesioNs and Patients Treated With Polymer Free Drug-CoatEd Stent ("Biofreedom"): the CHANCE a Multicenter Study

Acronym: CHANCE

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Aug 9, 2018
Registry last updated
Aug 9, 2018

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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