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Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial

BACKGROUND: The self-expandable COMPLETE™ stent (Medtronic) has greater elasticity, allowing it to regain its shape after the compression force reduces, and has higher trackability, thus is easier to maneuver through tortuous vessels, whereas the balloon-expandable SCUBA™ stent (Medtronic) has highe...

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Autores principales: Choi, Woong Gil, Rha, Seung Woon, Choi, Cheol Ung, Kim, Eung Ju, Oh, Dong Joo, Cho, Yoon Hyung, Park, Sang Ho, Lee, Seung Jin, Hur, Ae Yong, Ko, Young Guk, Park, Sang Min, Kim, Ki Chang, Kim, Joo Han, Kim, Min Woong, Kim, Sang Min, Bae, Jang Ho, Bong, Jung Min, Kang, Won Yu, Seo, Jae Bin, Jung, Woo Yong, Cho, Jang Hyun, Kim, Do Hoi, Ahn, Ji Hoon, Kim, Soo Hyun, Jang, Ji Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920989/
https://www.ncbi.nlm.nih.gov/pubmed/27344435
http://dx.doi.org/10.1186/s13063-016-1435-9
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author Choi, Woong Gil
Rha, Seung Woon
Choi, Cheol Ung
Kim, Eung Ju
Oh, Dong Joo
Cho, Yoon Hyung
Park, Sang Ho
Lee, Seung Jin
Hur, Ae Yong
Ko, Young Guk
Park, Sang Min
Kim, Ki Chang
Kim, Joo Han
Kim, Min Woong
Kim, Sang Min
Bae, Jang Ho
Bong, Jung Min
Kang, Won Yu
Seo, Jae Bin
Jung, Woo Yong
Cho, Jang Hyun
Kim, Do Hoi
Ahn, Ji Hoon
Kim, Soo Hyun
Jang, Ji Yong
author_facet Choi, Woong Gil
Rha, Seung Woon
Choi, Cheol Ung
Kim, Eung Ju
Oh, Dong Joo
Cho, Yoon Hyung
Park, Sang Ho
Lee, Seung Jin
Hur, Ae Yong
Ko, Young Guk
Park, Sang Min
Kim, Ki Chang
Kim, Joo Han
Kim, Min Woong
Kim, Sang Min
Bae, Jang Ho
Bong, Jung Min
Kang, Won Yu
Seo, Jae Bin
Jung, Woo Yong
Cho, Jang Hyun
Kim, Do Hoi
Ahn, Ji Hoon
Kim, Soo Hyun
Jang, Ji Yong
author_sort Choi, Woong Gil
collection PubMed
description BACKGROUND: The self-expandable COMPLETE™ stent (Medtronic) has greater elasticity, allowing it to regain its shape after the compression force reduces, and has higher trackability, thus is easier to maneuver through tortuous vessels, whereas the balloon-expandable SCUBA™ stent (Medtronic) has higher radial stiffness and can afford more accurate placement without geographic miss, which is important in aortoiliac bifurcation lesions. To date, there have been no randomized control trials comparing efficacy and safety between the self-expanding stent and balloon-expandable stent in advanced atherosclerotic iliac artery disease. METHODS/DESIGN: The purpose of our study is to examine primary patency (efficacy) and incidence of stent fracture and geographic miss (safety) between two different major representative stents, the self-expanding nitinol stent (COMPLETE-SE™) and the balloon-expanding cobalt-chromium stent (SCUBA™), in stenotic or occlusive iliac arterial lesions. This trial is designed as a prospective, randomized, multicenter trial to demonstrate a noninferiority of SCUBA™ stent to COMPLETE-SE™ stent following balloon angioplasty in iliac arterial lesions, and a total of 280 patients will be enrolled. The primary end point of this study is the rate of primary patency in the treated segment at 12 months after intervention as determined by catheter angiography, computed tomography angiography, or duplex ultrasound. DISCUSSION: The SENS-ILIAC trial will give powerful insight into whether the stent choice according to deployment mechanics would impact stent patency, geographic miss, or stent fracture in patients undergoing stent implantation in iliac artery lesions. TRIAL REGISTRATION: National Institutes of Health Clinical Trials Registry (ClinicalTrials.gov identifier: NCT01834495), registration date: May 8, 2012 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1435-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-49209892016-06-26 Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial Choi, Woong Gil Rha, Seung Woon Choi, Cheol Ung Kim, Eung Ju Oh, Dong Joo Cho, Yoon Hyung Park, Sang Ho Lee, Seung Jin Hur, Ae Yong Ko, Young Guk Park, Sang Min Kim, Ki Chang Kim, Joo Han Kim, Min Woong Kim, Sang Min Bae, Jang Ho Bong, Jung Min Kang, Won Yu Seo, Jae Bin Jung, Woo Yong Cho, Jang Hyun Kim, Do Hoi Ahn, Ji Hoon Kim, Soo Hyun Jang, Ji Yong Trials Study Protocol BACKGROUND: The self-expandable COMPLETE™ stent (Medtronic) has greater elasticity, allowing it to regain its shape after the compression force reduces, and has higher trackability, thus is easier to maneuver through tortuous vessels, whereas the balloon-expandable SCUBA™ stent (Medtronic) has higher radial stiffness and can afford more accurate placement without geographic miss, which is important in aortoiliac bifurcation lesions. To date, there have been no randomized control trials comparing efficacy and safety between the self-expanding stent and balloon-expandable stent in advanced atherosclerotic iliac artery disease. METHODS/DESIGN: The purpose of our study is to examine primary patency (efficacy) and incidence of stent fracture and geographic miss (safety) between two different major representative stents, the self-expanding nitinol stent (COMPLETE-SE™) and the balloon-expanding cobalt-chromium stent (SCUBA™), in stenotic or occlusive iliac arterial lesions. This trial is designed as a prospective, randomized, multicenter trial to demonstrate a noninferiority of SCUBA™ stent to COMPLETE-SE™ stent following balloon angioplasty in iliac arterial lesions, and a total of 280 patients will be enrolled. The primary end point of this study is the rate of primary patency in the treated segment at 12 months after intervention as determined by catheter angiography, computed tomography angiography, or duplex ultrasound. DISCUSSION: The SENS-ILIAC trial will give powerful insight into whether the stent choice according to deployment mechanics would impact stent patency, geographic miss, or stent fracture in patients undergoing stent implantation in iliac artery lesions. TRIAL REGISTRATION: National Institutes of Health Clinical Trials Registry (ClinicalTrials.gov identifier: NCT01834495), registration date: May 8, 2012 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1435-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-25 /pmc/articles/PMC4920989/ /pubmed/27344435 http://dx.doi.org/10.1186/s13063-016-1435-9 Text en © Choi et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Choi, Woong Gil
Rha, Seung Woon
Choi, Cheol Ung
Kim, Eung Ju
Oh, Dong Joo
Cho, Yoon Hyung
Park, Sang Ho
Lee, Seung Jin
Hur, Ae Yong
Ko, Young Guk
Park, Sang Min
Kim, Ki Chang
Kim, Joo Han
Kim, Min Woong
Kim, Sang Min
Bae, Jang Ho
Bong, Jung Min
Kang, Won Yu
Seo, Jae Bin
Jung, Woo Yong
Cho, Jang Hyun
Kim, Do Hoi
Ahn, Ji Hoon
Kim, Soo Hyun
Jang, Ji Yong
Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial
title Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial
title_full Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial
title_fullStr Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial
title_full_unstemmed Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial
title_short Study design and rationale of the ‘Balloon-Expandable Cobalt Chromium SCUBA Stent versus Self-Expandable COMPLETE-SE Nitinol Stent for the Atherosclerotic ILIAC Arterial Disease (SENS-ILIAC Trial) Trial’: study protocol for a randomized controlled trial
title_sort study design and rationale of the ‘balloon-expandable cobalt chromium scuba stent versus self-expandable complete-se nitinol stent for the atherosclerotic iliac arterial disease (sens-iliac trial) trial’: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920989/
https://www.ncbi.nlm.nih.gov/pubmed/27344435
http://dx.doi.org/10.1186/s13063-016-1435-9
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