Intervention with selution SLR™ Agent Balloon for Endovascular Latent Limus therapy for failing AV Fistulas (ISABELLA) Trial: Protocol for a pilot clinical study and pre-clinical results.
dc.contributor.author | Tang, Tjun Yip | |
dc.contributor.author | Chong, Tze-Tec | |
dc.contributor.author | Yap, Charyl Jia Qi | |
dc.contributor.author | Soon, Shereen Xue Yun | |
dc.contributor.author | Chan, Sze Ling | |
dc.contributor.author | Tan, Ru Yu | |
dc.contributor.author | Yap, Hao Yun | |
dc.contributor.author | Tay, Hsien Ts'ung | |
dc.contributor.author | Tan, Chieh-Suai | |
dc.contributor.author | Barnhill, Scott | |
dc.contributor.author | Hellinga, David | |
dc.contributor.author | DeGraw, R Tyler | |
dc.contributor.author | Finn, Aloke V | |
dc.date.accessioned | 2021-07-15T19:21:33Z | |
dc.date.available | 2021-07-15T19:21:33Z | |
dc.date.issued | 2021-07-03 | |
dc.identifier.uri | http://hdl.handle.net/10713/16191 | |
dc.description.abstract | The aim of this pilot clinical study is to evaluate the safety and efficacy of the Selution Sustained Limus Release (SLR)™ sirolimus-coated balloon (M.A. MedAlliance SA, Nyon, Switzerland) for improving the patency of failing arterio-venous fistulas (AVF) in hemodialysis patients. We also present herein a pre-clinical pharmacokinetic and safety evaluation of Selution™ to justify its first use in hemodialysis patients for endovascular access salvage. | en_US |
dc.description.uri | https://doi.org/10.1177/11297298211020867 | en_US |
dc.language.iso | en | en_US |
dc.publisher | SAGE Publications Inc. | en_US |
dc.relation.ispartof | Journal of Vascular Access | en_US |
dc.subject | Sirolimus coated balloon | en_US |
dc.subject | arterio-venous fistula | en_US |
dc.subject | outcome | en_US |
dc.subject | pre-clinical animal model | en_US |
dc.subject | safety | en_US |
dc.subject | target lesion primary patency | en_US |
dc.title | Intervention with selution SLR™ Agent Balloon for Endovascular Latent Limus therapy for failing AV Fistulas (ISABELLA) Trial: Protocol for a pilot clinical study and pre-clinical results. | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1177/11297298211020867 | |
dc.identifier.pmid | 34219511 | |
dc.source.beginpage | 11297298211020867 | |
dc.source.endpage | ||
dc.source.country | United States |