Effect of Bisoprolol on Progression of Aortic Stenosis (BLAST)
Primary Purpose
Aortic Stenosis
Status
Terminated
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
bisoprolol
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Aortic Stenosis focused on measuring aortic stenosis, beta-blocker
Eligibility Criteria
Inclusion Criteria:
- Mild to moderate aortic stenosis defined by peak velocity of aortic jet between 2.0 and 3.5 m/sec
- Untreated hypertension: systolic BP ≥ 140 or diastolic BP ≥ 90 mmHg Treated hypertension using dihydropiridine calcium channel blockers, ACE inhibitors, ARB or diuretics
- Patients received no beta-blocker therapy for more than 12 months
Exclusion Criteria:
- Symtomatic aortic stenosis: presence of exertional dyspnea, angina or syncope
- Planned cardiac surgery (e.g., CABG, valve repair or replacement, or aneurysmectomy) or planned major non-cardiac surgery within the study period
- Stroke or resuscitated sudden death in the past 6 months
- Evidence of congestive heart failure, or left ventricular ejection fraction < 50%
- Significant renal disease manifested by serum creatinine > 2.0mg/dL
- History of intolerance to beta-blocker
- History of adult asthma manifested by bronchospasm in the past 6 months, or currently taking regular anti-asthmatic medication(s)
- Moderate or severe aortic regurgitation
- Atrial fibrillation
- Female of child-bearing potential who do not use adequate contraception and women who are pregnant or breast-feeding
- A diagnosis of cancer (other than superficial squamous or basal cell skin cancer) in the past 3 years or current treatment for the active cancer
- Any clinically significant abnormality identified at the screening visit, physical examination, laboratory tests, or electrocardiogram which, in the judgment of the Investigator, would preclude safe completion of the study
- Unwillingness or inability to comply with the procedures described in this protocol
Sites / Locations
- Samsung Medical Center
- Asan Medical Center
- Seoul National University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
bisoprolol
placebo
Arm Description
bisoprolol 5mg qd
placebo
Outcomes
Primary Outcome Measures
Change in peak aortic jet velocity from baseline to 4 years follow-up
Change in peak aortic jet velocity from baseline to 4 years follow-up. For each patient, the change in peak aortic jet velocity is calculated as (peak aortic jet velocity at 4 year follow-up) - (peak aortic jet velocity at baseline) on Doppler echocardiography.
Secondary Outcome Measures
Change in mean pressure gradient across aortic valve
Change in mean pressure gradient across aortic valve from baseline to 4 years follow-up
Change in aortic valve area
Change in aortic valve area from baseline to 4 years follow-up
Change in BNP levels
Change in BNP levels from baseline to 4 years follow-up
Change in E/E' ratio
Change in the ratio of E velocity (early mitral inflow velocity) to E' velocity (early mitral annular velocity) from baseline to 4 years follow-up
Full Information
NCT ID
NCT01579058
First Posted
April 14, 2012
Last Updated
June 26, 2018
Sponsor
Asan Medical Center
Collaborators
Merck Sharp & Dohme LLC
1. Study Identification
Unique Protocol Identification Number
NCT01579058
Brief Title
Effect of Bisoprolol on Progression of Aortic Stenosis
Acronym
BLAST
Official Title
A Randomized Trial of Beta-blocker Therapy in Aortic Stenosis
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Terminated
Why Stopped
The sponsor discontinued to support the study.
Study Start Date
July 2012 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Asan Medical Center
Collaborators
Merck Sharp & Dohme LLC
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Aortic stenosis has been thought to be a degenerative process basically induced by long-lasting mechanical stress, and hemodynamic factors such as shear forces, acceleration of blood flow, hypertension and rapid heart rate might contribute to progression of aortic stenosis. Peak aortic jet velocity is known to be associated with clinical outcomes in mild and moderate AS, and our previous study showed that rate of progression was significantly associated with baseline aortic jet velocity in mild aortic stenosis. Because beta-blocker therapy would decrease aortic jet velocity and heart rate, it might decrease hemodynamic stress and eventually slow down the degenerative process in patients whose disease is not too advanced for therapy to be effective. The investigators hypothesized that a beta-blocker therapy would decrease the rate of progression of aortic stenosis by modifying hemodynamic factors favorably in patients with mild to moderate aortic stenosis.
Detailed Description
Aortic stenosis (AS) is a gradually progressive disease, characterized by an increase in calcium deposition leading to progressive narrowing of the aortic valve (AV). There are currently no effective medical treatment to halt the disease process and surgical valve replacement remains the only proven therapy when the valve becomes severely stenotic. AS is mediated by a chronic inflammatory disease process, very similar to that seen in atherosclerosis, but lipid-lowering therapy did not slow the progression of AS in the SALTIRE, SEAS, or ASTRONOMER trials. It is possible that these trials may have targeted patients in whom disease was too advanced for lipid-lowering therapy to be effective, or in whom atherosclerotic mechanism was not the central pathogenic process in AS. Because identifying and treating patients in earlier stages of AS would not be cost-effective, it seems more logical to explore alternative pharmacological approaches.
AS has been thought to be a degenerative process basically induced by long-lasting mechanical stress, and hemodynamic factors such as shear forces, acceleration of blood flow, hypertension and rapid heart rate might contribute to progression of AS. Peak aortic jet velocity is known to be associated with clinical outcomes in mild and moderate AS, and our previous study showed that rate of progression was significantly associated with baseline aortic jet velocity in mild AS. Because beta-blocker therapy would decrease aortic jet velocity and heart rate, it might decrease hemodynamic stress and eventually slow down the degenerative process in patients whose disease is not too advanced for therapy to be effective. In a retrospective, observational study, beta-blocker therapy was associated with a favorable clinical outcome in AS.
The investigators hypothesized that bisoprolol, a new generation beta-blocker, would decrease the rate of progression of AS by modifying hemodynamic factors favorably in patients with mild to moderate AS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Stenosis
Keywords
aortic stenosis, beta-blocker
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
bisoprolol
Arm Type
Active Comparator
Arm Description
bisoprolol 5mg qd
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
bisoprolol
Other Intervention Name(s)
Concor
Intervention Description
bisoprolol 5mg qd for 4 years
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo for 4 years
Primary Outcome Measure Information:
Title
Change in peak aortic jet velocity from baseline to 4 years follow-up
Description
Change in peak aortic jet velocity from baseline to 4 years follow-up. For each patient, the change in peak aortic jet velocity is calculated as (peak aortic jet velocity at 4 year follow-up) - (peak aortic jet velocity at baseline) on Doppler echocardiography.
Time Frame
4 years
Secondary Outcome Measure Information:
Title
Change in mean pressure gradient across aortic valve
Description
Change in mean pressure gradient across aortic valve from baseline to 4 years follow-up
Time Frame
4 years
Title
Change in aortic valve area
Description
Change in aortic valve area from baseline to 4 years follow-up
Time Frame
4 years
Title
Change in BNP levels
Description
Change in BNP levels from baseline to 4 years follow-up
Time Frame
4 years
Title
Change in E/E' ratio
Description
Change in the ratio of E velocity (early mitral inflow velocity) to E' velocity (early mitral annular velocity) from baseline to 4 years follow-up
Time Frame
4 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mild to moderate aortic stenosis defined by peak velocity of aortic jet between 2.0 and 3.5 m/sec
Untreated hypertension: systolic BP ≥ 140 or diastolic BP ≥ 90 mmHg Treated hypertension using dihydropiridine calcium channel blockers, ACE inhibitors, ARB or diuretics
Patients received no beta-blocker therapy for more than 12 months
Exclusion Criteria:
Symtomatic aortic stenosis: presence of exertional dyspnea, angina or syncope
Planned cardiac surgery (e.g., CABG, valve repair or replacement, or aneurysmectomy) or planned major non-cardiac surgery within the study period
Stroke or resuscitated sudden death in the past 6 months
Evidence of congestive heart failure, or left ventricular ejection fraction < 50%
Significant renal disease manifested by serum creatinine > 2.0mg/dL
History of intolerance to beta-blocker
History of adult asthma manifested by bronchospasm in the past 6 months, or currently taking regular anti-asthmatic medication(s)
Moderate or severe aortic regurgitation
Atrial fibrillation
Female of child-bearing potential who do not use adequate contraception and women who are pregnant or breast-feeding
A diagnosis of cancer (other than superficial squamous or basal cell skin cancer) in the past 3 years or current treatment for the active cancer
Any clinically significant abnormality identified at the screening visit, physical examination, laboratory tests, or electrocardiogram which, in the judgment of the Investigator, would preclude safe completion of the study
Unwillingness or inability to comply with the procedures described in this protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Duk-Hyun Kang, M.D.
Organizational Affiliation
Asan Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of
Facility Name
Asan Medical Center
City
Seoul
ZIP/Postal Code
138-736
Country
Korea, Republic of
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of
12. IPD Sharing Statement
Learn more about this trial
Effect of Bisoprolol on Progression of Aortic Stenosis
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