Effects of APIXaban on BRAIN Protection in Patients With Sinus Rhythm and Heart Failure: APIXBRAIN-HF Trial
Primary Purpose
Heart Failure, Sinus Rhythm, Cerebrovascular Disease
Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Apixaban
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring Heart failure, Sinus rhythm, NOAC, Brain
Eligibility Criteria
Inclusion Criteria:
- Patients aged over 19 years old
- Patients with sinus rhythm
Newly diagnosed of heart failure or aggravated heart failure symptom
- Dyspnea (≥ NYHA II)
- plasma BNP ≥ 200 pg/ml or NT-proBNP ≥ 800 pg/ml
LV systolic dysfunction on echocardiography within 3 month of enrollment
1) LVEF ≤ 40%
- Those with CHA2DS2-VASc ≥ 3
- Modified Rankin Score ≤ 4
Exclusion Criteria:
- Patients already subscribed warfarin or antiplatelet therapy or have clear indication for warfarin or antiplatelet therapy
- At high risk for bleeding
- Patients with atrial fibrillation
- Estimated glomerular filtration rate (CKD-EPI formula) < 15 ml/min/1.73 m2)
- Recent stroke or brain hemorrhage (within 3 months)
- Patients who was diagnosed of myocardial infarction or who has plan to PCI/CABG at enrollment
- End stage heart failure with life expectancy ≤ 6 months
- Patients with bed ridden status (Modified Rankin Score ≥ 5)
- Patients with liver dysfunction (AST, ALT > 2 times of upper normal limits or total bilirubin > 1.5 of upper normal limits)
- At of pregnancy or breastfeeding
- Patients who disagree with the use of medically acceptable contraception during the clinical trial period
- Patients with contraindication of apixaban
Sites / Locations
- Korea University Guro Hospital
- Korea University Ansan Hospital
- Chungnam National University Hospital
- Hallym University Dongtan Sacred Heart Hospital
- Seoul National University Bundang Hospital
- Korea University Anam Hospital
- Severance Hospital
- Asan Medical Center
- Samsung Medical Center
- Wonju Severance Christian Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Study group: apixaban
Control group: placebo
Arm Description
apixaban 2.5mg or 5mg bid
placebo bid
Outcomes
Primary Outcome Measures
New occurrence of brain pathology
1) Cortical cerebral microinfarcts 2) Silent lacunar infarction 3)Progression of white matter hyperintensities
Secondary Outcome Measures
The change of Mini-Mental State Examination-2 (MMSE-2) score
The change of Mini-Mental State Examination-2 (MMSE-2) score compared to baseline. Higher scores mean a better outcome.
New occurrence of cortical cerebral microinfarcts
New occurrence of cortical cerebral microinfarcts compared to baseline
New occurrence of silent lacunar infarction
New occurrence of silent lacunar infarction compared to baseline
Progression of white matter hyperintensities (more than 10% increase)
Progression of white matter hyperintensities (more than 10% increase) compared to baseline
Full Information
NCT ID
NCT04696120
First Posted
January 3, 2021
Last Updated
January 15, 2021
Sponsor
Korea University Guro Hospital
Collaborators
Dt&Sanomedics
1. Study Identification
Unique Protocol Identification Number
NCT04696120
Brief Title
Effects of APIXaban on BRAIN Protection in Patients With Sinus Rhythm and Heart Failure: APIXBRAIN-HF Trial
Official Title
Effects of APIXaban on BRAIN Protection in Patients With Sinus Rhythm and Heart Failure: APIXBRAIN-HF Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 2, 2021 (Anticipated)
Primary Completion Date
August 30, 2022 (Anticipated)
Study Completion Date
February 28, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea University Guro Hospital
Collaborators
Dt&Sanomedics
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
objectives: The primary aim of APIXBRAIN-HF Trial is to explore the effects of apixaban on brain protection in patients with sinus rhythm and heart failure
Primary / Secondary Endpoint
New occurrence of brain pathology 1) Cortical cerebral microinfarcts 2) Silent lacunar infarction 3)Progression of white matter hyperintensities
Secondary endpoint 1) The change of cognitive function evaluated by MMSE-2 2) Individual variable of primary endpoint
Safety Endpoint Evaluation 1) Cerebral microbleeds on imaging
Detailed Description
This study is a double-blind, parallel-group, and randomization study. The investigators will enroll the patients with heart failure who demonstrated LV systolic dysfunction (LVEF ≤ 40%) and sinus rhythm with a CHA2DS2-VASc score ≥ 3. All patients would be randomly assigned to either the apixaban group or placebo group. Patients assigned to the apixaban group will receive 5mg bid or 2.5mg bid (patients with at least 2 of the following characteristics: aged≥80-year, bodyweight ≤60kg, serum creatinine 1.5 ml/dL) and patients in the placebo group will receive a placebo of apixaban. Both drugs will be maintained for 6 months. During the study period, all patients will be carefully monitored for thromboembolic events, including stroke. At the beginning of the study and 6 months after randomization, 3T Brain MRI and MMSE-2 test will be performed to identify changes in brain structure and cognitive function.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Sinus Rhythm, Cerebrovascular Disease
Keywords
Heart failure, Sinus rhythm, NOAC, Brain
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Study group: apixaban
Arm Type
Experimental
Arm Description
apixaban 2.5mg or 5mg bid
Arm Title
Control group: placebo
Arm Type
Placebo Comparator
Arm Description
placebo bid
Intervention Type
Drug
Intervention Name(s)
Apixaban
Other Intervention Name(s)
apixaban 5mg or 2.5mg bid
Intervention Description
Patients who are randomly assigned to apixaban group will receive apixaban 5mg or 2.5mg bid
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
placebo bid
Intervention Description
All patients who are assigned to placebo group will receive placebo
Primary Outcome Measure Information:
Title
New occurrence of brain pathology
Description
1) Cortical cerebral microinfarcts 2) Silent lacunar infarction 3)Progression of white matter hyperintensities
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
The change of Mini-Mental State Examination-2 (MMSE-2) score
Description
The change of Mini-Mental State Examination-2 (MMSE-2) score compared to baseline. Higher scores mean a better outcome.
Time Frame
24 weeks
Title
New occurrence of cortical cerebral microinfarcts
Description
New occurrence of cortical cerebral microinfarcts compared to baseline
Time Frame
24 weeks
Title
New occurrence of silent lacunar infarction
Description
New occurrence of silent lacunar infarction compared to baseline
Time Frame
24 weeks
Title
Progression of white matter hyperintensities (more than 10% increase)
Description
Progression of white matter hyperintensities (more than 10% increase) compared to baseline
Time Frame
24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients aged over 19 years old
Patients with sinus rhythm
Newly diagnosed of heart failure or aggravated heart failure symptom
Dyspnea (≥ NYHA II)
plasma BNP ≥ 200 pg/ml or NT-proBNP ≥ 800 pg/ml
LV systolic dysfunction on echocardiography within 3 month of enrollment
1) LVEF ≤ 40%
Those with CHA2DS2-VASc ≥ 3
Modified Rankin Score ≤ 4
Exclusion Criteria:
Patients already subscribed warfarin or antiplatelet therapy or have clear indication for warfarin or antiplatelet therapy
At high risk for bleeding
Patients with atrial fibrillation
Estimated glomerular filtration rate (CKD-EPI formula) < 15 ml/min/1.73 m2)
Recent stroke or brain hemorrhage (within 3 months)
Patients who was diagnosed of myocardial infarction or who has plan to PCI/CABG at enrollment
End stage heart failure with life expectancy ≤ 6 months
Patients with bed ridden status (Modified Rankin Score ≥ 5)
Patients with liver dysfunction (AST, ALT > 2 times of upper normal limits or total bilirubin > 1.5 of upper normal limits)
At of pregnancy or breastfeeding
Patients who disagree with the use of medically acceptable contraception during the clinical trial period
Patients with contraindication of apixaban
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eung Ju Kim, MD, PhD
Phone
82-02-2626-3022
Email
withnoel@empas.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jah Yeon Choi, MD, PhD
Email
kekeruki@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eung Ju Kim, MD, PhD.
Organizational Affiliation
Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Korea University Guro Hospital
City
Seoul
State/Province
Guro-gu
ZIP/Postal Code
08308
Country
Korea, Republic of
Facility Name
Korea University Ansan Hospital
City
Ansan
ZIP/Postal Code
15355
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sung Hwan Kim, MD,PhD.
Email
echoshkim@gmail.com
Facility Name
Chungnam National University Hospital
City
Daejeon
ZIP/Postal Code
35015
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jin Ok Cheong, MD,PhD.
Email
jojeong@cnu.ac.kr
Facility Name
Hallym University Dongtan Sacred Heart Hospital
City
Hwaseong-si
ZIP/Postal Code
18450
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Seong Woo Han, MD,PhD.
Email
hansw29@hanmail.net
Facility Name
Seoul National University Bundang Hospital
City
Seongnam-si
ZIP/Postal Code
13620
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dong ju Choi, MD,PhD.
Email
djchoi@snubh.org
First Name & Middle Initial & Last Name & Degree
Jin Joo Park, MD,PhD.
Email
65755@snubh.org
Facility Name
Korea University Anam Hospital
City
Seoul
ZIP/Postal Code
02841
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sung Mi Park, MD,PhD.
Email
smparkmd@korea.ac.kr
First Name & Middle Initial & Last Name & Degree
Mi-Na Kim, MD,PhD.
Email
alsk1229@gmail.com
Facility Name
Severance Hospital
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Seok Min Kang, MD,PhD.
Email
SMKANG@yuhs.ac
First Name & Middle Initial & Last Name & Degree
Jaewon Oh, MD,PhD.
Email
ericjcoh@yuhs.ac
Facility Name
Asan Medical Center
City
Seoul
ZIP/Postal Code
05505
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Min Seok Kim, MD,PhD.
Email
guess124@gmail.com
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
06351
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jin Oh Choi, MD,PhD.
Email
choijean5@gmail.com
Facility Name
Wonju Severance Christian Hospital
City
Wonju
ZIP/Postal Code
26426
Country
Korea, Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Byeong Soo Yoo, MD,PhD.
Email
yubs@yonsei.ac.kr
12. IPD Sharing Statement
Plan to Share IPD
No
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Effects of APIXaban on BRAIN Protection in Patients With Sinus Rhythm and Heart Failure: APIXBRAIN-HF Trial
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