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
About this trial
This is an interventional treatment trial for Aortic Valve Stenosis
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
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
NCT ID
NCT03001960
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
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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