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Adjunctive Treatment With Doxycycline to Enhance the Durability of Endovascular Aortic Aneurysm Repair

Primary Purpose

Aortic Aneurysm

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Doxycycline
Sponsored by
The Foundation for Barnes-Jewish Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Aneurysm focused on measuring endoleak, doxycycline, matrix metalloproteinase, inflammation, endograft, circulating markers

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Presence of an abdominal aortic aneurysm (AAA) with a maximum diameter of > or = 4.5 cm Planned aneurysm exclusion with endoluminal stent graft (any brand) Exclusion Criteria: Known malignancy not to include prostate cancer or any history of cancer that has not had a recurrence in the last 5 years. Hypersensitivity to doxycycline or any of its components Pregnancy Ruptured AAA Extension of covered portion of the graft above the renal arteries Previous endoluminal aneurysm repair

Sites / Locations

  • Washington University School of Medicine / Barnes-Jewish Hospital

Outcomes

Primary Outcome Measures

Change in aortic measurements by > 2 mm on 2 consecutive scans
Change in aortic measurement by > 5 mm on a single scan
50% reduction in baseline plasma MMP-9 at 6 months

Secondary Outcome Measures

Significant reductions at 6 months in serum interleukin-6 (IL-6)
Significant reductions at 6 months in serum IL-8
Significant reductions at 6 months in serum interferon-gamma
Significant reductions at 6 months in serum C-reactive protein

Full Information

First Posted
August 2, 2005
Last Updated
March 3, 2010
Sponsor
The Foundation for Barnes-Jewish Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00126204
Brief Title
Adjunctive Treatment With Doxycycline to Enhance the Durability of Endovascular Aortic Aneurysm Repair
Official Title
Adjunctive Treatment With Doxycycline in Endovascular Aneurysm Repair
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Completed
Study Start Date
March 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
The Foundation for Barnes-Jewish Hospital

4. Oversight

5. Study Description

Brief Summary
The durability of endovascular aneurysm repair (EVAR) has been limited by development of endoleaks which may be secondary to progressive aortic degeneration by matrix metalloproteases (MMP). Doxycycline is a known inhibitor of the MMP family of enzymes in aneurysms. The investigators propose a randomized, controlled trial of adjuvant doxycycline therapy with EVAR to determine its effects on re-intervention, aneurysm shrinkage and serum markers of aneurysmal degeneration.
Detailed Description
Patients will be consented and enrolled at the time of their clinic visit or admission to the hospital for a planned EVAR, in accordance with institutional review board guidelines. Demographic, risk factor and medication regimen data will be obtained from the patient's clinical chart. Patients will be randomized to doxycycline therapy (100 mg taken twice daily) or a placebo. The patients will receive their first dose of study medication on the day following surgery, and continue the study therapy for 6 months. Plasma and serum will be obtained at the time of enrollment (baseline), and at each post-operative follow-up visit during the study as outlined above. Aliquots will be stored at -80ºC until assayed. Measurements of the circulating markers will be performed by commercially available assays for plasma MMP-9 (R&D Systems, Minneapolis, MN), serum IL-6 (R&D Systems) , IL-8 (R&D Systems), IFN-gamma (R&D Systems), and CRP (Bio-Check, Burlingame, CA) Data will be collected from the pre-operative and all post-operative CT scans regarding maximal aneurysm diameter and transverse neck diameter at 5 mm, 10 mm and 15 mm below the takeoff of the lowest renal artery. All documented endoleaks and their clinical type will be recorded, as will any re-intervention related to the graft or aneurysm. The primary end-points of the study related to aneurysm measurements will be an increase or decrease in any of the diameter measurements of the aorta by 2 mm or more on 2 consecutive CT scans or a change of 5 mm or more on any single scan. Of the circulating markers, an additional primary endpoint will be a 50% reduction in baseline MMP-9 after endografting. Secondary endpoints will be significant reductions over baseline in circulating IL-6, IL-8, IFN-γ, and CRP. An a priori power analysis indicates that at 6 months, reductions in circulating levels of these markers by 50% can be detected with a β-error of less than 0.1 and α-error of less than 0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Aneurysm
Keywords
endoleak, doxycycline, matrix metalloproteinase, inflammation, endograft, circulating markers

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
75 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Doxycycline
Primary Outcome Measure Information:
Title
Change in aortic measurements by > 2 mm on 2 consecutive scans
Title
Change in aortic measurement by > 5 mm on a single scan
Title
50% reduction in baseline plasma MMP-9 at 6 months
Secondary Outcome Measure Information:
Title
Significant reductions at 6 months in serum interleukin-6 (IL-6)
Title
Significant reductions at 6 months in serum IL-8
Title
Significant reductions at 6 months in serum interferon-gamma
Title
Significant reductions at 6 months in serum C-reactive protein

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Presence of an abdominal aortic aneurysm (AAA) with a maximum diameter of > or = 4.5 cm Planned aneurysm exclusion with endoluminal stent graft (any brand) Exclusion Criteria: Known malignancy not to include prostate cancer or any history of cancer that has not had a recurrence in the last 5 years. Hypersensitivity to doxycycline or any of its components Pregnancy Ruptured AAA Extension of covered portion of the graft above the renal arteries Previous endoluminal aneurysm repair
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John A Curci, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine / Barnes-Jewish Hospital
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18632241
Citation
Hackmann AE, Rubin BG, Sanchez LA, Geraghty PA, Thompson RW, Curci JA. A randomized, placebo-controlled trial of doxycycline after endoluminal aneurysm repair. J Vasc Surg. 2008 Sep;48(3):519-26; discussion 526. doi: 10.1016/j.jvs.2008.03.064. Epub 2008 Jul 15.
Results Reference
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Adjunctive Treatment With Doxycycline to Enhance the Durability of Endovascular Aortic Aneurysm Repair

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