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Comparison of Beta-blocker Versus Angiotensin Receptor Blocker for Suppression of Aneurysm Expansion in Patients With Small Abdominal Aortic Aneurysm and Hypertension (BASE Trial)

Primary Purpose

Small Abdominal Aortic Aneurysm

Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Beta-blocker-Atenolol 50mg, PO(peroral), Once daily
Angiotensin receptor blocker-Valsartan 80mg, PO(peroral), Once daily
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Small Abdominal Aortic Aneurysm

Eligibility Criteria

20 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥20years
  • Abdominal aortic aneurysm with maximal diameter less than 5cm
  • Hypertension
  • Patient with signed informed consent

Exclusion Criteria:

  • Saccular type aneurysm, inflammatory aneurysm, or infected aneurysm
  • Aortic dissection
  • Planned surgery or endovascular therapy for abdominal aortic aneurysm within 1 year
  • Previous aorta surgery or endovascular therapy
  • Contraindications to Beta-blocker or ARB (allergic reactions, asthma, severe bradycardia, angioedema, hyperkalemia)
  • Allergic reaction to contrast dye
  • Known genetic aorta disease or autoimmune or connective tissue disease: Marfan syndrome, Shprintzen-Goldberg syndrome, Loeys-Dietz syndrome, Takayasu's arteritis, Behcet's disease
  • Pregnancy
  • Life expectation <1 year
  • Renal failure (serum Cr >2.0 mg/dL)
  • Liver disease (ALT or AST > 3 x upper limit) or liver cirrhosis (Child B or C)
  • Malignancy requiring surgery or chemotherapy within 1 year after enrollment
  • Status post transplantation or chronic inflammatory disease requiring immune suppressive drugs over 4 weeks

Sites / Locations

  • Severance Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Atenolol

Valsartan

Arm Description

Atenolol group

Valsartan group

Outcomes

Primary Outcome Measures

Annual aneurysm growth of abdominal aortic aneurysm

Secondary Outcome Measures

Full Information

First Posted
July 17, 2013
Last Updated
March 26, 2019
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT01904981
Brief Title
Comparison of Beta-blocker Versus Angiotensin Receptor Blocker for Suppression of Aneurysm Expansion in Patients With Small Abdominal Aortic Aneurysm and Hypertension (BASE Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
April 18, 2017 (Actual)
Study Completion Date
April 18, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Various medical therapies have been proposed to prevent abdominal aortic aneurysm expansion. However, there have been very few randomized clinical trials to support use of any of these treatments. Several animal studies and observational reports suggest that ARBs can be useful in reducing abdominal aortic aneurysm (AAA) growth. However, so far, ARBs have not been evaluated in a randomized clinical trial. Therefore, the purpose of the study is to evaluate the effect of valsartan, an ARB, on annual growth rate in comparison with atenolol, a beta-blocker. Our hypothesis is that valsartan is superior to atenolol in the suppression of the aneurysm growth at 12 months. The BASE trial is designed as a investigator-initiated, multi-center, randomized controlled open-label trial. Patients with small AAA (aorta diameter <5cm) will be randomized 1:1 either to valsartan or to atenolol group. Randomization will be stratified by the AAA size (max. diameter >4 cm or ≤4 cm). Patients will receive either valsartan (daily dose 80 mg or more) or atenolol (daily dose 50 mg or more) for 12 months. A CT scan will measure the maximal diameter of AAA at baseline and 12 months. The annual growth of AAA will be compared between the valsartan and the atenolol group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Small Abdominal Aortic Aneurysm

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Atenolol
Arm Type
Experimental
Arm Description
Atenolol group
Arm Title
Valsartan
Arm Type
Experimental
Arm Description
Valsartan group
Intervention Type
Drug
Intervention Name(s)
Beta-blocker-Atenolol 50mg, PO(peroral), Once daily
Intervention Type
Drug
Intervention Name(s)
Angiotensin receptor blocker-Valsartan 80mg, PO(peroral), Once daily
Primary Outcome Measure Information:
Title
Annual aneurysm growth of abdominal aortic aneurysm
Time Frame
at 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥20years Abdominal aortic aneurysm with maximal diameter less than 5cm Hypertension Patient with signed informed consent Exclusion Criteria: Saccular type aneurysm, inflammatory aneurysm, or infected aneurysm Aortic dissection Planned surgery or endovascular therapy for abdominal aortic aneurysm within 1 year Previous aorta surgery or endovascular therapy Contraindications to Beta-blocker or ARB (allergic reactions, asthma, severe bradycardia, angioedema, hyperkalemia) Allergic reaction to contrast dye Known genetic aorta disease or autoimmune or connective tissue disease: Marfan syndrome, Shprintzen-Goldberg syndrome, Loeys-Dietz syndrome, Takayasu's arteritis, Behcet's disease Pregnancy Life expectation <1 year Renal failure (serum Cr >2.0 mg/dL) Liver disease (ALT or AST > 3 x upper limit) or liver cirrhosis (Child B or C) Malignancy requiring surgery or chemotherapy within 1 year after enrollment Status post transplantation or chronic inflammatory disease requiring immune suppressive drugs over 4 weeks
Facility Information:
Facility Name
Severance Hospital
City
Seoul
ZIP/Postal Code
120-752
Country
Korea, Republic of

12. IPD Sharing Statement

Learn more about this trial

Comparison of Beta-blocker Versus Angiotensin Receptor Blocker for Suppression of Aneurysm Expansion in Patients With Small Abdominal Aortic Aneurysm and Hypertension (BASE Trial)

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