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Azelnidipine Anti-Coronary Atherosclerotic Trial in Hypertensive Patients by Serial Volumetric IVUS Analysis(ALPS-J)

Primary Purpose

Hypertension, Coronary Atherosclerosis

Status
Completed
Phase
Phase 4
Locations
Japan
Study Type
Interventional
Intervention
Calcium channel blockers (amlodipine, azelnidipine)
Sponsored by
Juntendo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension focused on measuring Hypertension, PCI, Calcium Channel Blockers, IVUS, Plaque

Eligibility Criteria

20 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age: Between 20 and 79 years (at the time of giving informed consent). Sex: Either sex. Admission status: Outpatients. Patients requiring treatment for hypertension according to the JSH 2004 hypertension therapy guidelines before beginning this study Patients who have not used any calcium antagonists for at least 4 weeks before the beginning of this study. Patients who are scheduled to undergo elective PCI. Exclusion Criteria: Patients with acute coronary syndrome (ACS). Patients who have experienced Q-wave myocardial infarction within 4 weeks before beginning this study. Patients with renal dysfunction (serum creatinine >2.0 mg/dL). Patients in whom PCI is unsuccessful. Patients with cardiogenic shock. Patients with moderate or severe congestive heart failure. Patients with 50% or more stenosis of the main trunk of the left coronary artery. Patients with other problems whom the investigator considers unsuitable for this study.

Sites / Locations

  • Department of Cardiology, Juntendo University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Amlodipine

Azelnidipine

Outcomes

Primary Outcome Measures

Percent change in plaque volume from the baseline value. (IVUS) Percent change in plaque volume = (plaque volume after 48 weeks of drug administration - baseline plaque volume) / baseline plaque volume

Secondary Outcome Measures

Change of plaque volume from the baseline value. (IVUS) Amount change and percent change in Minimal lumen diameter and % stenosis. (Quantitative Coronary Analysis) Change of intimal thickening volume in-stent.
Correlativity of plaque volume and inflammatory laboratory parameters (hs-CRP, MCP-1, PTX-3) Correlativity of laboratory parameters and blood pressure. Correlativity of plaque volume and antioxidant laboratory parameters (LPO, 8-isoprostane)
The following treatments and incidence of events, Changes from baseline of laboratory parameters (TC, LDL-C,TG, HDL-C, hs-CRP, MCP-1, LPO, 8-isoprostane, PTX-3) after 48 weeks of drug administration. Correlativity of plaque volume and blood pressure.

Full Information

First Posted
February 20, 2006
Last Updated
May 12, 2021
Sponsor
Juntendo University
Collaborators
Japan Heart Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00294567
Brief Title
Azelnidipine Anti-Coronary Atherosclerotic Trial in Hypertensive Patients by Serial Volumetric IVUS Analysis(ALPS-J)
Official Title
Azelnidipine and Amlodipine Anti-Coronary Atherosclerotic Trial in Hypertensive Patients Undergoing Coronary Intervention by Serial Volumetric Intravascular Ultrasound Analysis in Junten Medical University (ALPS-J)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2008
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
January 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Juntendo University
Collaborators
Japan Heart Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In patients with hypertension who undergo elective PCI, the effects of long-term administration of Calblock (azelnidipine) on plaque volume will be determined quantitatively by 3D-IVUS and compared with those of amlodipine besilate (Norvasc or Amlodin).
Detailed Description
Clinical studies have demonstrated that calcium antagonists can reduce cardiovascular events in patients with coronary artery disease. Recently, suppression of the development of coronary atherosclerotic plaque by calcium antagonists has been reported as one of the mechanisms involved. Thus, calcium antagonists have been promising strategy for preventing the progression of the coronary atherosclerosis. Various calcium antagonists are clinically available at present and these drugs may differ from each other with respect to the anti-atherosclerotic effects. Consequently, we plan to perform the ALPS-J study to compare the effects of two long-acting calcium antagonists, azelnidipine and amlodipine, on plaque quantitatively by IVUS. In this study, azelnidipine (16 mg/day) or amlodipine besilate (5 mg/day) will be administered to patients with hypertension for 48 weeks after elective PCI. The plaque volume will be measured in each patient by IVUS at the time of PCI and 48 weeks after PCI. Percent change in plaque volume from the baseline value will be used as the primary endpoints for evaluation of efficacy. We plan to enroll 100 patients in each group for a total of 200 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Coronary Atherosclerosis
Keywords
Hypertension, PCI, Calcium Channel Blockers, IVUS, Plaque

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
199 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Amlodipine
Arm Title
2
Arm Type
Active Comparator
Arm Description
Azelnidipine
Intervention Type
Drug
Intervention Name(s)
Calcium channel blockers (amlodipine, azelnidipine)
Intervention Description
Drug: amlodipine Drug: azelnidipine
Primary Outcome Measure Information:
Title
Percent change in plaque volume from the baseline value. (IVUS) Percent change in plaque volume = (plaque volume after 48 weeks of drug administration - baseline plaque volume) / baseline plaque volume
Time Frame
48Weeks
Secondary Outcome Measure Information:
Title
Change of plaque volume from the baseline value. (IVUS) Amount change and percent change in Minimal lumen diameter and % stenosis. (Quantitative Coronary Analysis) Change of intimal thickening volume in-stent.
Time Frame
48Weeks
Title
Correlativity of plaque volume and inflammatory laboratory parameters (hs-CRP, MCP-1, PTX-3) Correlativity of laboratory parameters and blood pressure. Correlativity of plaque volume and antioxidant laboratory parameters (LPO, 8-isoprostane)
Time Frame
48Weeks
Title
The following treatments and incidence of events, Changes from baseline of laboratory parameters (TC, LDL-C,TG, HDL-C, hs-CRP, MCP-1, LPO, 8-isoprostane, PTX-3) after 48 weeks of drug administration. Correlativity of plaque volume and blood pressure.
Time Frame
48Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: Between 20 and 79 years (at the time of giving informed consent). Sex: Either sex. Admission status: Outpatients. Patients requiring treatment for hypertension according to the JSH 2004 hypertension therapy guidelines before beginning this study Patients who have not used any calcium antagonists for at least 4 weeks before the beginning of this study. Patients who are scheduled to undergo elective PCI. Exclusion Criteria: Patients with acute coronary syndrome (ACS). Patients who have experienced Q-wave myocardial infarction within 4 weeks before beginning this study. Patients with renal dysfunction (serum creatinine >2.0 mg/dL). Patients in whom PCI is unsuccessful. Patients with cardiogenic shock. Patients with moderate or severe congestive heart failure. Patients with 50% or more stenosis of the main trunk of the left coronary artery. Patients with other problems whom the investigator considers unsuitable for this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
HIROYUKI MD DAIDA
Organizational Affiliation
Director of Cardiology Professor of Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Cardiology, Juntendo University School of Medicine
City
Tokyo
Country
Japan

12. IPD Sharing Statement

Citations:
PubMed Identifier
23214115
Citation
Miyauchi K, Daida H. [Azelnidipine and amlodipine anti-coronary atherosclerosis trial in hypertensive patients undergoing coronary intervention by serial volumetric intravascular ultrasound analysis in Juntendo Medical University]. Nihon Naika Gakkai Zasshi. 2012 Oct 10;101(10):3002-11. doi: 10.2169/naika.101.3002. No abstract available. Japanese.
Results Reference
derived
PubMed Identifier
21471671
Citation
Kojima T, Miyauchi K, Yokoyama T, Yokoyama K, Kurata T, Suwa S, Kawamura M, Tamura H, Okazaki S, Inoue K, Fujiwara Y, Sumiyoshi M, Tanimoto K, Nakazato Y, Yamagami S, Hiro T, Komiyama N, Daida H. Azelnidipine and amlodipine anti-coronary atherosclerosis trial in hypertensive patients undergoing coronary intervention by serial volumetric intravascular ultrasound analysis in Juntendo University (ALPS-J). Circ J. 2011;75(5):1071-9. doi: 10.1253/circj.cj-11-0141. Epub 2011 Apr 7.
Results Reference
derived

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Azelnidipine Anti-Coronary Atherosclerotic Trial in Hypertensive Patients by Serial Volumetric IVUS Analysis(ALPS-J)

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