Adjunctive Treatment With Doxycycline to Enhance the Durability of Endovascular Aortic Aneurysm Repair
NCT ID: NCT00126204
Last Updated: 2010-03-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
75 participants
INTERVENTIONAL
2004-03-31
2006-07-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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Doxycycline
Eligibility Criteria
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Inclusion Criteria
* Planned aneurysm exclusion with endoluminal stent graft (any brand)
Exclusion Criteria
* 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
50 Years
ALL
No
Sponsors
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The Foundation for Barnes-Jewish Hospital
OTHER
Principal Investigators
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John A Curci, MD
Role: PRINCIPAL_INVESTIGATOR
Washington University School of Medicine
Locations
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Washington University School of Medicine / Barnes-Jewish Hospital
St Louis, Missouri, United States
Countries
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References
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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.
Other Identifiers
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00012-0904-02
Identifier Type: -
Identifier Source: org_study_id
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