Global Iliac Branch Study

NCT ID: NCT05607277

Last Updated: 2024-04-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

297 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-11-30

Study Completion Date

2021-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This project seeks to determine if certain anatomic factors, specifically tortuous and non-conformable iliac arteries, may predict device complications, including seal zone failure, type III endoleak, and occlusion. Approximately 400 subjects from 5 academic centers across the United States, Europe, and Asia will be included in this study. Various markers of pre- and post-treatment iliac anatomy will be measured using CT imaging, and clinical events will be reported by academic centers. The relationship of imaging data to patient demographics will then be assessed alongside anatomic and demographic predictors of non-conformability.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Background and significance Abdominal aortic aneurysms (AAAs) affect 0.5% to 1.3% of women and 4.0% to 7.6% of men age 65 and older1-4. Infrarenal AAAs frequently extend distally through the aortic bifurcation and into the common, external, and/or internal iliac arteries,5,6 presenting a challenge for aneurysm repair. Current guidelines prioritize repair strategies which preserve blood flow to the internal iliac artery (IIA) with the goal of reducing the complications of buttock claudication and pelvic ischemia.7-9 As endovascular intervention has become standard practice for those with eligible anatomy, 7 branched endovascular devices have been developed to preserve IIA blood flow when repairing AAAs with iliac involvement.

With the ongoing development of devices and techniques, the range of iliac anatomy eligible for endovascular repair has increased. Most notably, multiple iliac branch devices (IBDs) are being used to treat AAAs involving highly tortuous iliac arteries. A variety of IBDs are available globally, and as such, there is an opportunity to determine if certain anatomic factors- specifically tortuous and non-conformable iliac arteries- may predict device complications.

To begin exploring this question, the Global Iliac Branch Study (GIBS)- a partnership between 5 centers across the United States, Europe, and Asia- was developed to evaluate performance of branched endografts based on anatomical assessments, with analysis of CT scans using centralized and standardized analysis protocols at the AortaCore Imaging Lab at the University of Wisconsin-Madison.

Previous work In addition to elevated risk of conversion to open repair,10 iliac tortuosity has previously been associated with increased risk of "conformability" events, including seal zone failure, type III endoleak, occlusion, stenosis, compression, and device migration.11-13

Previously, the applicant and her faculty mentor have explored the interaction between iliac tortuosity and device conformability in patients treated with the W.L.GORE EXCLUDER iliac branch endoprosthesis (IBE).14 Non-conformation was defined as a decrease in the total iliac index of tortuosity beyond 15%. This study found that non-conformation, as well as internal iliac artery diameter of less than 10 mm, were associated with adverse iliac events after iliac branch endoprosthesis (odds ratio, 8.2 \[P = .02\] and odds ratio, 12.3 \[P = .02\], respectively).

Similar to the aforementioned studies demonstrating increasing ranges of anatomic eligibility with the development of more complex and accommodating devices, the applicant and her mentor explored device eligibility for endovascular repair (EVAR) of small AAA over two years in a paper published in November 2021 in the Journal of Vascular Surgery which found high levels of anatomic eligibility for EVAR at baseline, and preservation of this eligibility over two years.15 These findings, like those previously mentioned, suggested that advancements in EVAR device design have improved anatomic eligibility for the procedure. Compared to open repair, EVAR is associated with decreased periprocedural morbidity and hospital length of stay,16 and as such is the preferred approach, as well as a major target for innovation in the field of vascular surgery.

Methods and analysis CT images of 400 subjects with IBDs from 5 centers around the globe will be transferred and analyzed at the University of Wisconsin-Madison AortaCore Imaging Lab under an Institutional Review Board (IRB) approved protocol. Post-processing workstations using Aquarius Intuition (version 4.4.12, TeraRecon) will be used to measure morphology data. Each CT will be fit with a manually corrected centerline that is equidistant from the outer walls of the aneurysmal vessels. Measurements will be completed at both the pre-treatment and post-treatment intervals; these include common, external, and internal iliac artery diameters and lengths, common iliac artery index of tortuosity (Common Iliac Index; Centerline length of the common iliac artery (CIA) divided by the shortest straight-line distance between the CIA origin and iliac bifurcation), total iliac artery index of tortuosity (Total Iliac Index; centerline length of the CIA plus centerline length of the external iliac artery, divided by the shortest straight-line distance between the CIA origin and terminal external iliac artery), and presence of the double iliac sign (when any portion of the iliac vessel is tortuous enough to be duplicated in a single cut of an axial computed tomography slice.)17 Figures 1 and 2 demonstrate these measurement techniques for capturing and quantifying tortuosity.

Measurement of these values before and after device deployment allows the determination of differences in iliac artery length pre- and post-treatment, which is used to quantify device "conformability."18 Notably, devices which produce minimal changes to native anatomy are considered more "conformable" and devices that make greater changes to iliac lengths and angle anatomy are considered "non-conformable" (Figure 3.)

In addition to pre-treatment demographics and comorbidities, including age, sex, and geographic origin, associations between iliac tortuosity indices and the aforementioned CT measurements will be determined in relation to clinical events collected by each center including conversion to open repair, re-intervention, endoleak, occlusion, compression, patient-reported symptoms and adverse events, and death.

Continuous variables will be compared using the unpaired Student t test if normally distributed and the Mann-Whitney U test or Wilcoxon matched pairs test if they are not normally distributed. Categorical variables will be compared using the Fisher exact test or Pearson's x2 test.

Expected outcomes As previously described, in preliminary data14 we have identified that a postoperative change in iliac tortuosity ("non-conformability") predicts adverse events in a sample size of 98 patients. We hypothesize that a larger sample size of 400 patients will confirm this relationship between non-conformability and adverse events, and enable identification of pre-operative predictors of non-conformability. Furthermore, we anticipate that the inclusion of a more diverse selection of endovascular devices will more broadly capture the relationship between device conformability and iliac tortuosity beyond what can be determined based on commercially available devices in the United States.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Abdominal Aortic Aneurysm Iliac Aneurysm

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Endovascular Repair of abdominal aortic aneurysms

Femoral artery access

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Endovascular repair of abdominal aorto-iliac aneurysm

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Subjects who have undergone endovascular aortic repair of AAA with iliac involvement via iliac branch device.

Exclusion Criteria

* None
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Wisconsin, Madison

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jon Matsumura, MD

Role: PRINCIPAL_INVESTIGATOR

University of Wisconsin, Madison

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Wisconsin

Madison, Wisconsin, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

Chichester Aneurysm Screening Group; Viborg Aneurysm Screening Study; Western Australian Abdominal Aortic Aneurysm Program; Multicentre Aneurysm Screening Study. A comparative study of the prevalence of abdominal aortic aneurysms in the United Kingdom, Denmark, and Australia. J Med Screen. 2001;8(1):46-50. doi: 10.1136/jms.8.1.46.

Reference Type BACKGROUND
PMID: 11373850 (View on PubMed)

Derubertis BG, Trocciola SM, Ryer EJ, Pieracci FM, McKinsey JF, Faries PL, Kent KC. Abdominal aortic aneurysm in women: prevalence, risk factors, and implications for screening. J Vasc Surg. 2007 Oct;46(4):630-635. doi: 10.1016/j.jvs.2007.06.024.

Reference Type BACKGROUND
PMID: 17903646 (View on PubMed)

US Preventive Services Task Force; Owens DK, Davidson KW, Krist AH, Barry MJ, Cabana M, Caughey AB, Doubeni CA, Epling JW Jr, Kubik M, Landefeld CS, Mangione CM, Pbert L, Silverstein M, Simon MA, Tseng CW, Wong JB. Screening for Abdominal Aortic Aneurysm: US Preventive Services Task Force Recommendation Statement. JAMA. 2019 Dec 10;322(22):2211-2218. doi: 10.1001/jama.2019.18928.

Reference Type BACKGROUND
PMID: 31821437 (View on PubMed)

Svensjo S, Bjorck M, Wanhainen A. Current prevalence of abdominal aortic aneurysm in 70-year-old women. Br J Surg. 2013 Feb;100(3):367-72. doi: 10.1002/bjs.8984. Epub 2012 Nov 28.

Reference Type BACKGROUND
PMID: 23192439 (View on PubMed)

Ghosh J, Murray D, Paravastu S, Farquharson F, Walker MG, Serracino-Inglott F. Contemporary management of aorto-iliac aneurysms in the endovascular era. Eur J Vasc Endovasc Surg. 2009 Feb;37(2):182-8. doi: 10.1016/j.ejvs.2008.11.001. Epub 2008 Nov 29.

Reference Type BACKGROUND
PMID: 19046903 (View on PubMed)

Maurel B, Bartoli MA, Jean-Baptiste E, Reix T, Cardon A, Goueffic Y, Martinez R, Cochennec F, Albertini JN, Chauffour X, Steinmetz E, Haulon S; Association Universitaire de Recherche en Chirurgie Vasculaire, France. Perioperative evaluation of iliac ZBIS branch devices: a French multicenter study. Ann Vasc Surg. 2013 Feb;27(2):131-8. doi: 10.1016/j.avsg.2011.02.052.

Reference Type BACKGROUND
PMID: 23380549 (View on PubMed)

Chaikof EL, Dalman RL, Eskandari MK, Jackson BM, Lee WA, Mansour MA, Mastracci TM, Mell M, Murad MH, Nguyen LL, Oderich GS, Patel MS, Schermerhorn ML, Starnes BW. The Society for Vascular Surgery practice guidelines on the care of patients with an abdominal aortic aneurysm. J Vasc Surg. 2018 Jan;67(1):2-77.e2. doi: 10.1016/j.jvs.2017.10.044.

Reference Type BACKGROUND
PMID: 29268916 (View on PubMed)

Faries PL, Morrissey N, Burks JA, Gravereaux E, Kerstein MD, Teodorescu VJ, Hollier LH, Marin ML. Internal iliac artery revascularization as an adjunct to endovascular repair of aortoiliac aneurysms. J Vasc Surg. 2001 Nov;34(5):892-9. doi: 10.1067/mva.2001.118085.

Reference Type BACKGROUND
PMID: 11700492 (View on PubMed)

Kouvelos GN, Katsargyris A, Antoniou GA, Oikonomou K, Verhoeven EL. Outcome after Interruption or Preservation of Internal Iliac Artery Flow During Endovascular Repair of Abdominal Aorto-iliac Aneurysms. Eur J Vasc Endovasc Surg. 2016 Nov;52(5):621-634. doi: 10.1016/j.ejvs.2016.07.081. Epub 2016 Sep 2.

Reference Type BACKGROUND
PMID: 27600731 (View on PubMed)

Cuypers PW, Laheij RJ, Buth J. Which factors increase the risk of conversion to open surgery following endovascular abdominal aortic aneurysm repair? The EUROSTAR collaborators. Eur J Vasc Endovasc Surg. 2000 Aug;20(2):183-9. doi: 10.1053/ejvs.2000.1167.

Reference Type BACKGROUND
PMID: 10944101 (View on PubMed)

Iwakoshi S, Nakai T, Ichihashi S, Inoue T, Sakaguchi S, Hirose T, Tabayashi N, Watkins AC, Kichikawa K. Conformability and Efficacy of the Zenith Spiral Z Leg Compared with the Zenith Flex Leg in Endovascular Abdominal Aortic Aneurysm Repair. Ann Vasc Surg. 2019 Aug;59:127-133. doi: 10.1016/j.avsg.2019.02.013. Epub 2019 May 7.

Reference Type BACKGROUND
PMID: 31071429 (View on PubMed)

Wolf YG, Tillich M, Lee WA, Rubin GD, Fogarty TJ, Zarins CK. Impact of aortoiliac tortuosity on endovascular repair of abdominal aortic aneurysms: evaluation of 3D computer-based assessment. J Vasc Surg. 2001 Oct;34(4):594-9. doi: 10.1067/mva.2001.118586.

Reference Type BACKGROUND
PMID: 11668310 (View on PubMed)

Parra JR, Ayerdi J, McLafferty R, Gruneiro L, Ramsey D, Solis M, Hodgson K. Conformational changes associated with proximal seal zone failure in abdominal aortic endografts. J Vasc Surg. 2003 Jan;37(1):106-11. doi: 10.1067/mva.2002.53.

Reference Type BACKGROUND
PMID: 12514585 (View on PubMed)

DeRoo E, Harris D, Olson S, Panthofer A, Meadows W, Pauli T, Peterson B, Schneider D, Matsumura J. Conformability of the GORE EXCLUDER iliac branch endoprosthesis is associated with freedom from adverse iliac events. J Vasc Surg. 2021 Nov;74(5):1558-1564.e1. doi: 10.1016/j.jvs.2021.05.026. Epub 2021 Jun 1.

Reference Type BACKGROUND
PMID: 34082005 (View on PubMed)

Panthofer AM, Olson SL, Rademacher BL, Grudzinski JK, Chaikof EL, Matsumura JS; N-TA(3)CT Investigators. Anatomic eligibility for endovascular aneurysm repair preserved over 2 years of surveillance. J Vasc Surg. 2021 Nov;74(5):1527-1536.e1. doi: 10.1016/j.jvs.2021.04.044. Epub 2021 May 4.

Reference Type BACKGROUND
PMID: 33957227 (View on PubMed)

Olson SL, Panthofer AM, Harris DJ, Jordan WD Jr, Farber MA, Cambria RP, Matsumura JS. CT-Derived Pretreatment Thoracic Sarcopenia Is Associated with Late Mortality after Thoracic Endovascular Aortic Repair. Ann Vasc Surg. 2020 Jul;66:171-178. doi: 10.1016/j.avsg.2019.10.089. Epub 2019 Nov 6.

Reference Type BACKGROUND
PMID: 31705993 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

A539750

Identifier Type: OTHER

Identifier Source: secondary_id

SMPH/SURGERY/VASCULAR SURGERY

Identifier Type: OTHER

Identifier Source: secondary_id

Protocol Version 7/29/2020

Identifier Type: OTHER

Identifier Source: secondary_id

2020-0677

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Genomics of In-Stent Restenosis
NCT00341562 COMPLETED
DURABILITY™ Iliac Study
NCT01400919 COMPLETED NA
VISIBILITY™ Iliac Study
NCT01402700 COMPLETED NA
The GORE® VIABAHN® FORTEGRA Venous Stent IVC Study
NCT05409976 ACTIVE_NOT_RECRUITING NA