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Dual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in TAVI (DAPT-TAVI)

Primary Purpose

Aortic Valve Stenosis, Transcatheter Aortic Valve Replacement, Intracranial Embolism

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Preloading before TAVI
Postloading after TAVI
Sponsored by
Charite University, Berlin, Germany
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Valve Stenosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Patients >18 years and <90 years
  • Patients undergoing TF-TAVI for severe aortic stenosis (combined with aortic regurgitation)
  • Informed consent

Exclusion criteria:

  • TIA/Stroke within last 90 days
  • Aortic valve-in-valve procedures
  • TAVI for treatment of isolated aortic regurgitation
  • known significant carotid stenosis (>70%)
  • Prior myocardial infarction or revascularization with PCI or CABG within past 3 months
  • Clopidogrel and/ or Aspirin within past 7 days
  • any other indication for (dual) antiplatelet therapy
  • Contraindication to MRI (MRI conditional pacemakers accepted!)
  • participation in another interventional trial
  • cardiogenic shock (positive shock index OR need for catecholamine support OR systolic bloodpressure < 90 mmHg) or need for pre-hospital intubation
  • cardiac arrest <90 days prior to randomization
  • Pregnant or lactating females

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    Group 1- PREloading BEFORE TAVI

    Group 2 - POSTLoading AFTER TAVI

    Arm Description

    Aspirin 100 mg loading orally 6-12 hours before TAVI and Clopidogrel 600mg loading 6-12 before TAVI followed by maintenance dose of 100mg aspirin and 75mg clopidogrel per day

    Aspirin 100 mg loading orally 6-12 hours after TAVI and Clopidogrel 600mg loading 6-12 hours after TAVI followed by maintenance dose of 100mg aspirin and 75mg clopidogrel per day

    Outcomes

    Primary Outcome Measures

    Total volume of new cerebral lesions on MRI after TAVI versus Baseline

    Secondary Outcome Measures

    New lesion volume of cerebral embolization in patients treated with ASS and Clopidogrel before versus after TAVI
    Total new lesion volume is defined as the sum volume of all new cerebral ischemic lesions on the post-procedural MRI relative to the pre-TAVR cerebral MRI scan (on diffusion weighted and FLAIR MRI images).
    location of new cerebral lesions early AFTER TAVI
    To evaluate cerebral embolisation, which is not procedure related, cerebral embolisation on MRI will be before TAVI versus the post-TAVI MRI scan
    extent of new cerebral lesions early AFTER TAVI
    To evaluate cerebral embolisation, which is not procedure related, cerebral embolisation on MRI will be before TAVI versus the post-TAVI MRI scan
    Assessment of different neurocognitive tests before and after TAVI procedure
    To evaluate neurologic function with a battery of neurocognitive tests and to correlate these findings to cerebral MRI scans
    Extent of clinically apparent non-cerebral emboli after TAVI
    To describe extent and localization of non-cerebral embolisation (e.g. pulmonary embolism, limb ischaemia...)
    localization of clinically apparent non-cerebral emboli after TAVI
    To describe extent and localization of non-cerebral embolisation (e.g. pulmonary embolism, limb ischaemia...)
    Evaluation of possible changes in quality of life after TAVI with EQ-5D questionnaire sum score.

    Full Information

    First Posted
    December 18, 2016
    Last Updated
    December 27, 2016
    Sponsor
    Charite University, Berlin, Germany
    Collaborators
    Prof. Dr. Jochen Fiebach, Center for Stroke Research Berlin (CSB), Charité - Universitaetsmedizin Berlin
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03001960
    Brief Title
    Dual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in TAVI
    Acronym
    DAPT-TAVI
    Official Title
    Dual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in Transcatheter Aortic Valve Implantation (TAVI)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    March 2017 (undefined)
    Primary Completion Date
    March 2018 (Anticipated)
    Study Completion Date
    April 2018 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Charite University, Berlin, Germany
    Collaborators
    Prof. Dr. Jochen Fiebach, Center for Stroke Research Berlin (CSB), Charité - Universitaetsmedizin Berlin

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    TAVI is increasingly adopted as standard treatment for many subgroups of patients with aortic stenosis. However, due to a lack of data there is yet no TAVI-specific guidance regarding the optimum periinterventional drug regimen. The study evaluates the effect of dual antiplatelet pretreatment on periinterventional embolic cerebral lesions and bleeding complications in patients undergoing transfemoral aortic valve implantation (TF-TAVI).
    Detailed Description
    Patients undergoing TAVI bear a high risk of ischaemic stroke, which is an independent predictor of mortality1. Dual antiplatelet therapy (DAPT) is recommended by current guidelines without clear specifications on the time of initiation of treatment due to a lack of data. While some centers initiate DAPT with aspirin and clopidogrel prior to TAVI to reduce the rate of periinterventional embolic events, others start these medications after the procedure.Data on antithrombotic therapy during TAVI are scarce and no randomized evaluation has been performed to demonstrate what the best strategy is during the procedure. Therefore, the objective of this clinical trial is to assess the efficacy of pre- versus postoperative dual antiplatelet loading with Aspirin and Clopidogrel on volume of periinterventional cerebral ischemic lesions as quantified by diffusion weight MRI (DW-MRI) and neurocognitive function in patients undergoing transfemoral aortic valve replacement. The statistical trial design assumes superiority of preloading with DAPT regarding the primary endpoint.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Aortic Valve Stenosis, Transcatheter Aortic Valve Replacement, Intracranial Embolism

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Group 1- PREloading BEFORE TAVI
    Arm Type
    Experimental
    Arm Description
    Aspirin 100 mg loading orally 6-12 hours before TAVI and Clopidogrel 600mg loading 6-12 before TAVI followed by maintenance dose of 100mg aspirin and 75mg clopidogrel per day
    Arm Title
    Group 2 - POSTLoading AFTER TAVI
    Arm Type
    Experimental
    Arm Description
    Aspirin 100 mg loading orally 6-12 hours after TAVI and Clopidogrel 600mg loading 6-12 hours after TAVI followed by maintenance dose of 100mg aspirin and 75mg clopidogrel per day
    Intervention Type
    Drug
    Intervention Name(s)
    Preloading before TAVI
    Other Intervention Name(s)
    ASS, Plavix
    Intervention Description
    Preloading with Aspirin and Clopidogrel before TAVI
    Intervention Type
    Drug
    Intervention Name(s)
    Postloading after TAVI
    Other Intervention Name(s)
    ASS, Plavix
    Intervention Description
    Postloading with Aspirin and Clopidogrel after TAVI
    Primary Outcome Measure Information:
    Title
    Total volume of new cerebral lesions on MRI after TAVI versus Baseline
    Time Frame
    Total volume of new cerebral lesions on MRI, 24-72h after TAV versus Baseline
    Secondary Outcome Measure Information:
    Title
    New lesion volume of cerebral embolization in patients treated with ASS and Clopidogrel before versus after TAVI
    Description
    Total new lesion volume is defined as the sum volume of all new cerebral ischemic lesions on the post-procedural MRI relative to the pre-TAVR cerebral MRI scan (on diffusion weighted and FLAIR MRI images).
    Time Frame
    24-72h post TAVI versus baseline
    Title
    location of new cerebral lesions early AFTER TAVI
    Description
    To evaluate cerebral embolisation, which is not procedure related, cerebral embolisation on MRI will be before TAVI versus the post-TAVI MRI scan
    Time Frame
    24-72h after TAVI
    Title
    extent of new cerebral lesions early AFTER TAVI
    Description
    To evaluate cerebral embolisation, which is not procedure related, cerebral embolisation on MRI will be before TAVI versus the post-TAVI MRI scan
    Time Frame
    24-72h after TAVI
    Title
    Assessment of different neurocognitive tests before and after TAVI procedure
    Description
    To evaluate neurologic function with a battery of neurocognitive tests and to correlate these findings to cerebral MRI scans
    Time Frame
    24-72 h after TAVI
    Title
    Extent of clinically apparent non-cerebral emboli after TAVI
    Description
    To describe extent and localization of non-cerebral embolisation (e.g. pulmonary embolism, limb ischaemia...)
    Time Frame
    24-72 h after TAVI
    Title
    localization of clinically apparent non-cerebral emboli after TAVI
    Description
    To describe extent and localization of non-cerebral embolisation (e.g. pulmonary embolism, limb ischaemia...)
    Time Frame
    24-72 h after TAVI
    Title
    Evaluation of possible changes in quality of life after TAVI with EQ-5D questionnaire sum score.
    Time Frame
    24-72 h after TAVI

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: Patients >18 years and <90 years Patients undergoing TF-TAVI for severe aortic stenosis (combined with aortic regurgitation) Informed consent Exclusion criteria: TIA/Stroke within last 90 days Aortic valve-in-valve procedures TAVI for treatment of isolated aortic regurgitation known significant carotid stenosis (>70%) Prior myocardial infarction or revascularization with PCI or CABG within past 3 months Clopidogrel and/ or Aspirin within past 7 days any other indication for (dual) antiplatelet therapy Contraindication to MRI (MRI conditional pacemakers accepted!) participation in another interventional trial cardiogenic shock (positive shock index OR need for catecholamine support OR systolic bloodpressure < 90 mmHg) or need for pre-hospital intubation cardiac arrest <90 days prior to randomization Pregnant or lactating females

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    25756438
    Citation
    Holmes DR Jr, Brennan JM, Rumsfeld JS, Dai D, O'Brien SM, Vemulapalli S, Edwards FH, Carroll J, Shahian D, Grover F, Tuzcu EM, Peterson ED, Brindis RG, Mack MJ; STS/ACC TVT Registry. Clinical outcomes at 1 year following transcatheter aortic valve replacement. JAMA. 2015 Mar 10;313(10):1019-28. doi: 10.1001/jama.2015.1474.
    Results Reference
    background
    PubMed Identifier
    23727214
    Citation
    Osnabrugge RL, Mylotte D, Head SJ, Van Mieghem NM, Nkomo VT, LeReun CM, Bogers AJ, Piazza N, Kappetein AP. Aortic stenosis in the elderly: disease prevalence and number of candidates for transcatheter aortic valve replacement: a meta-analysis and modeling study. J Am Coll Cardiol. 2013 Sep 10;62(11):1002-12. doi: 10.1016/j.jacc.2013.05.015. Epub 2013 May 30.
    Results Reference
    background

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    Dual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in TAVI

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