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Trial record 1 of 2 for:    DESSOLVE III
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Study Comparing the MiStent SES Versus the XIENCE EES Stent (DESSOLVE III)

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ClinicalTrials.gov Identifier: NCT02385279
Recruitment Status : Unknown
Verified December 2020 by ECRI bv.
Recruitment status was:  Active, not recruiting
First Posted : March 11, 2015
Last Update Posted : December 19, 2020
Micell Technologies
Information provided by (Responsible Party):

Brief Summary:
The primary objective of this study is to compare the performance of MISTENT to that of XIENCE in an all-comers patient population with symptomatic ischemic heart disease. The patients will be followed through 3 years for major clinical events.

Condition or disease Intervention/treatment Phase
Coronary Stenosis Device: MiStent Device: XIENCE EES Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 1404 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Multicenter Randomized Study of the MiStent Sirolimus Eluting Absorbable Polymer Stent System (MiStent SES) for Revascularization of Coronary Arteries
Actual Study Start Date : March 20, 2015
Actual Primary Completion Date : January 31, 2017
Estimated Study Completion Date : January 2021

Arm Intervention/treatment
Experimental: MiStent®
Percutaneous Coronary Intervention with the MiStent Sirolimus Eluting Absorbable Polymer Coronary Stent. It is a balloon expandable sirolimus eluting stent with an absorbable polymer coating.
Device: MiStent
Percutaneous Coronary Intervention

Active Comparator: XIENCE EES
Percutaneous Coronary Intervention with the XIENCE EES (Everolimus Eluting) Coronary Stent System. The stents are balloon expandable drug eluting stents using everolimus with a non-erodible or durable polymer coating.
Percutaneous Coronary Intervention

Primary Outcome Measures :
  1. Non inferiority comparison of a device oriented composite endpoint (DOCE) or Target Lesion Failure (TLF) of the MISTENT group to the XIENCE group [ Time Frame: 12 months postprocedure ]
    TLF is a composite of clinical endpoint of cardiac death, myocardial infarction not clearly attributable to a nontarget vessel and clinically-indicated target lesion revascularization.

Secondary Outcome Measures :
  1. POCE defined as all-cause death, any Myocardial Infarction (MI), or any revascularization [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]
  2. MACE defined as all-cause death, any MI, or any Target Vessel Revascularization (TVR) [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]
  3. Target Vessel Failure (TVF) defined as cardiac death, TV MI, or clinically indicated TVR [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]
  4. DOCE/TLF defined as cardiac death, TV MI or clinically indicated Target Lesion Revascularization (TLR) [ Time Frame: 30 days, 6 months, 2 years, 3 years ]
  5. Mortality [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]
  6. Myocardial infarction [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]
  7. Revascularization [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]
  8. Stent thrombosis rates according to ARC classification [ Time Frame: 30 days, 6 months, 1 year, 2 years and 3 years ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

All comers" patients:

  • Male or female patients 18 years or older;
  • Presence of one or more coronary artery stenoses of 50% or more in a native coronary artery or in a saphenous venous or arterial bypass conduit suitable for coronary stent implantation.
  • The vessel should have a reference vessel diameter ranging from 2.5 mm to 3.75 mm (no limitation on the number of treated lesions, vessels, or lesion length); All lesions of the patient must comply with the angiographic inclusion criteria.
  • The patient is judged to be capable of providing voluntary informed consent and has been fully informed of the nature of the study, is willing to comply with all study requirements and will provide written informed consent as approved by the Ethics Committee of the respective clinical site.

Exclusion Criteria:

  • Known pregnancy or breastfeeding at time of randomization;
  • Known contraindication or hypersensitivity to sirolimus, everolimus, cobalt-chromium, or to medications such as aspirin, heparin, bivalirudin, and all of the following four medications: clopidogrel bisulfate, ticlopidine, prasugrel, ticagrelor;
  • Concurrent medical condition with a life expectancy of less than 12 months.
  • The patient is unwilling/ not able to return for outpatient clinic at 1 month and 12 months follow-up.
  • Currently participating in another trial and not yet at its primary endpoint.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02385279

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Sponsors and Collaborators
Micell Technologies
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Principal Investigator: P. W. Serruys, Prof. MD. International Center for Circulatory Health, NHLI, Imperial College, London, United Kingdom
Principal Investigator: W Wijns, Prof. MD. Hartcenter, OLV Aalst, Belgium
Principal Investigator: R. de Winter, Prof. MD. Academisch Medisch Centrum, Amsterdam, The Netherlands
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: ECRI bv
ClinicalTrials.gov Identifier: NCT02385279    
Other Study ID Numbers: ECRI-005
First Posted: March 11, 2015    Key Record Dates
Last Update Posted: December 19, 2020
Last Verified: December 2020
Keywords provided by ECRI bv:
All comers
Additional relevant MeSH terms:
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Coronary Stenosis
Coronary Disease
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases