Dual Antiplatelet Therapy Versus Oral Anticoagulation for a Short Time to Prevent Cerebral Embolism After TAVI (AUREA)
Primary Purpose
Aortic Valve Stenosis, Stroke
Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
aspirin+clopidogrel (Duoplavin)
Sponsored by
About this trial
This is an interventional treatment trial for Aortic Valve Stenosis focused on measuring Antiplatelet, Anticoagulation
Eligibility Criteria
Inclusion Criteria:
- Adult patients (more than 18 years) with ability to understand and accept the participation in the clinical trial.
- Patients with symptomatic degenerative severe aortic stenosis rejected for conventional surgical aortic valve replacement due to unacceptably high risk and accepted for TAVI procedure
- Signed informed consent.
- Patients who are not participating in any other clinical trial or research study.
Exclusion Criteria:
- Patients under oral anticoagulation treatment
- Patients who can not undergo MRI study
- Recent stroke < 14 days prior, revascularized coronary artery disease or life expectancy < 12 months
- Patients with proven allergy to aspirin, clopidogrel or acenocoumarol
- Patients that after TAVI procedure can not undergo a regimen of dual antiplatelet therapy or oral anticoagulation for 3 months due to any new post-TAVI medical indication
Sites / Locations
- Policlínica de Guipuzcoa.SA
- Hospital Universitario Álvaro Cunqueiro
- Hospital clinico Universitario Bellvitge
- Hospital Clinico Universitario de Malaga
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Duoplavin
acenocumarol
Arm Description
Both active substances in DuoPlavin: clopidogrel and acetylsalicylic acid, are inhibitors of platelet aggregation. Clopidogrel stops the platelets aggregating by blocking ADP. Acetylsalicylic acid the platelets aggregating by blocking the prostaglandin cyclo oxygenase.
Outcomes
Primary Outcome Measures
Evaluate the effectiveness of dual antiplatelet therapy versus oral anticoagulation for prevention of cerebral thromboembolism by the detection of new areas of cerebral infarction by Magnetic Resonance Imaging (MRI) 3 months after TAVI.
Secondary Outcome Measures
Determine the incidence of new areas of cerebral infarction by MRI between the different routes of vascular access and the various valve devices.
Identify the development of cognitive impairment after TAVI
By the application of: 1)Mini-Mental State Examination (MMSE); 2)SF 36 (spanish version); 3)The NIHSS (National Institute of Health Stroke Scale). The evaluation of the neurological tests will be performed by a certificated neurologist.
Evaluate the Quality of life after TAVI.
By the application of Euroquol EQ5.
Full Information
NCT ID
NCT01642134
First Posted
June 19, 2012
Last Updated
August 8, 2019
Sponsor
Andres Iñiguez Romo, MD, PhD
1. Study Identification
Unique Protocol Identification Number
NCT01642134
Brief Title
Dual Antiplatelet Therapy Versus Oral Anticoagulation for a Short Time to Prevent Cerebral Embolism After TAVI
Acronym
AUREA
Official Title
PHASE IV Study of Dual Antiplatelet Therapy Versus Oral Anticoagulation for a Short Time to Prevent Cerebral Embolism After Percutaneous Aortic Valve Implantation. Multicenter Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Andres Iñiguez Romo, MD, PhD
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the incidence of major vascular events (ischemic or haemorrhagics) at the third month after initiation of the antithrombotic treatment (oral anticoagulation or dual antiplatelet therapy) in both arms followed TAVI.
Detailed Description
Transcatheter aortic valve implantation (TAVI) procedure using any of their vascular access is an option with proven benefit definitively for treatment of severe symptomatic aortic stenosis in patients considered unsuitable for conventional open heart surgery.
By avoiding the hemodynamic effects, cardiovascular and cerebral microembolic load of cardiopulmonary bypass circulation, it is assumed that the TAVI procedure is beneficial despite the risk of neurological complications. Currently antithrombotic therapy after the procedure is not standardized. International treatment guidelines recommends that post-operative patients with a conventional surgical aortic bioprosthesis maintain oral anticoagulation for 3 months after the procedure, unless otherwise noted for its continuation. Whereas some studies have postulated that in patients with aortic bioprostheses, dual antiplatelet therapy is as effective to prevent major cardiac and cerebrovascular events as oral anticoagulation, with a lower incidence of bleeding complications at 3 months of treatment, the investigators formulated the following hypothesis:
• There is a lower incidence of major cardiac and cerebrovascular events in patients with dual antiplatelet therapy compared to patients with oral anticoagulation for 3 months after implantation of an aortic bioprosthesis TAVI procedure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Valve Stenosis, Stroke
Keywords
Antiplatelet, Anticoagulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
124 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Duoplavin
Arm Type
Active Comparator
Arm Description
Both active substances in DuoPlavin: clopidogrel and acetylsalicylic acid, are inhibitors of platelet aggregation. Clopidogrel stops the platelets aggregating by blocking ADP. Acetylsalicylic acid the platelets aggregating by blocking the prostaglandin cyclo oxygenase.
Arm Title
acenocumarol
Arm Type
Sham Comparator
Intervention Type
Drug
Intervention Name(s)
aspirin+clopidogrel (Duoplavin)
Other Intervention Name(s)
DUOPLAVIN (aspirin 100 mg + clopidogrel 75 mg)., SINTROM (ACENOCUMAROL).
Intervention Description
100 mg aspirin ;75 mg clopidogrel 3º months
Primary Outcome Measure Information:
Title
Evaluate the effectiveness of dual antiplatelet therapy versus oral anticoagulation for prevention of cerebral thromboembolism by the detection of new areas of cerebral infarction by Magnetic Resonance Imaging (MRI) 3 months after TAVI.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Determine the incidence of new areas of cerebral infarction by MRI between the different routes of vascular access and the various valve devices.
Time Frame
1 hour before TAVI, 1 hour and 24 hours after TAVI
Title
Identify the development of cognitive impairment after TAVI
Description
By the application of: 1)Mini-Mental State Examination (MMSE); 2)SF 36 (spanish version); 3)The NIHSS (National Institute of Health Stroke Scale). The evaluation of the neurological tests will be performed by a certificated neurologist.
Time Frame
Pre-TAVI, and at 1º 3º and 6º month after TAVI
Title
Evaluate the Quality of life after TAVI.
Description
By the application of Euroquol EQ5.
Time Frame
Pre-TAVI, and at 1º; 3º and 6º month after TAVI.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients (more than 18 years) with ability to understand and accept the participation in the clinical trial.
Patients with symptomatic degenerative severe aortic stenosis rejected for conventional surgical aortic valve replacement due to unacceptably high risk and accepted for TAVI procedure
Signed informed consent.
Patients who are not participating in any other clinical trial or research study.
Exclusion Criteria:
Patients under oral anticoagulation treatment
Patients who can not undergo MRI study
Recent stroke < 14 days prior, revascularized coronary artery disease or life expectancy < 12 months
Patients with proven allergy to aspirin, clopidogrel or acenocoumarol
Patients that after TAVI procedure can not undergo a regimen of dual antiplatelet therapy or oral anticoagulation for 3 months due to any new post-TAVI medical indication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andres Iniguez Romo, MD;PHD
Organizational Affiliation
Hospital Universitario Alvaro Cunqueiro
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Victor A. Jimenez Diaz, MD;Msc
Organizational Affiliation
Hospital clinico universitario Vigo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mariano Larman Tellechea, MD
Organizational Affiliation
Policlínica de Guipuzcoa SA San Sebastián
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pablo Juan Salvadores, Pharma,MPH
Organizational Affiliation
Hospital Universitario Álvaro Cunqueiro
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jose M. Hernandez, MD
Organizational Affiliation
Hospital Virgen de la Victoria
Official's Role
Principal Investigator
Facility Information:
Facility Name
Policlínica de Guipuzcoa.SA
City
San Sebastián
State/Province
Guipúzcoa
ZIP/Postal Code
20014
Country
Spain
Facility Name
Hospital Universitario Álvaro Cunqueiro
City
Vigo
State/Province
Pontevedra
ZIP/Postal Code
36312
Country
Spain
Facility Name
Hospital clinico Universitario Bellvitge
City
Barcelona
ZIP/Postal Code
36201
Country
Spain
Facility Name
Hospital Clinico Universitario de Malaga
City
Malaga
ZIP/Postal Code
36201
Country
Spain
12. IPD Sharing Statement
Citations:
PubMed Identifier
21639811
Citation
Smith CR, Leon MB, Mack MJ, Miller DC, Moses JW, Svensson LG, Tuzcu EM, Webb JG, Fontana GP, Makkar RR, Williams M, Dewey T, Kapadia S, Babaliaros V, Thourani VH, Corso P, Pichard AD, Bavaria JE, Herrmann HC, Akin JJ, Anderson WN, Wang D, Pocock SJ; PARTNER Trial Investigators. Transcatheter versus surgical aortic-valve replacement in high-risk patients. N Engl J Med. 2011 Jun 9;364(23):2187-98. doi: 10.1056/NEJMoa1103510. Epub 2011 Jun 5.
Results Reference
background
PubMed Identifier
20961243
Citation
Leon MB, Smith CR, Mack M, Miller DC, Moses JW, Svensson LG, Tuzcu EM, Webb JG, Fontana GP, Makkar RR, Brown DL, Block PC, Guyton RA, Pichard AD, Bavaria JE, Herrmann HC, Douglas PS, Petersen JL, Akin JJ, Anderson WN, Wang D, Pocock S; PARTNER Trial Investigators. Transcatheter aortic-valve implantation for aortic stenosis in patients who cannot undergo surgery. N Engl J Med. 2010 Oct 21;363(17):1597-607. doi: 10.1056/NEJMoa1008232. Epub 2010 Sep 22.
Results Reference
background
PubMed Identifier
20177005
Citation
Kahlert P, Knipp SC, Schlamann M, Thielmann M, Al-Rashid F, Weber M, Johansson U, Wendt D, Jakob HG, Forsting M, Sack S, Erbel R, Eggebrecht H. Silent and apparent cerebral ischemia after percutaneous transfemoral aortic valve implantation: a diffusion-weighted magnetic resonance imaging study. Circulation. 2010 Feb 23;121(7):870-8. doi: 10.1161/CIRCULATIONAHA.109.855866.
Results Reference
background
PubMed Identifier
11062293
Citation
Herrmann M, Vos P, Wunderlich MT, de Bruijn CH, Lamers KJ. Release of glial tissue-specific proteins after acute stroke: A comparative analysis of serum concentrations of protein S-100B and glial fibrillary acidic protein. Stroke. 2000 Nov;31(11):2670-7. doi: 10.1161/01.str.31.11.2670.
Results Reference
background
PubMed Identifier
18375137
Citation
Dunning J, Versteegh M, Fabbri A, Pavie A, Kolh P, Lockowandt U, Nashef SA; EACTS Audit and Guidelines Committee. Guideline on antiplatelet and anticoagulation management in cardiac surgery. Eur J Cardiothorac Surg. 2008 Jul;34(1):73-92. doi: 10.1016/j.ejcts.2008.02.024. Epub 2008 Mar 28. Erratum In: Eur J Cardiothorac Surg. 2008 Oct;34(4):934.
Results Reference
background
Links:
URL
http://www.cardiologia-vigo.com/
Description
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Dual Antiplatelet Therapy Versus Oral Anticoagulation for a Short Time to Prevent Cerebral Embolism After TAVI
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