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临床试验/NCT03763812
NCT03763812撤回不适用

Explorative Study on the Inflammatory Response After Endovascular Aortic Aneurysm Repair and Endovascular Aneurysm Sealing.

Rijnstate Hospital7 个研究点 分布在 5 个国家开始时间: 2019年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
7
主要终点
Change in inflammatory response between EVAS and EVAR

研究概览

简要总结

Retrospective data have shown that active sac management, as applied in EVAS, reduces the incidence of the post-implant syndrome. All-cause and cardiac mortality at one-year seems to be lower after EVAS when compared to EVAR. Ongoing, low grade, inflammation could differ between techniques and induce cardiac damage.

This study is designed to establish whether EVAS results in a reduced post-operative inflammatory response during the first year after surgery, compared to EVAR as assessed by trends in circulating inflammatory cytokine concentration.

Study design: International prospective, comparative, explorative study. Study population: Patients scheduled to undergo infra-renal EVAR with a polyester endograft or EVAS for an infrarenal aortic aneurysm. This is an explorative study and therefore only patients who would normally receive a suitable device as part of standard treatment at the participating institutes will be recruited. Blood samples will be taken at specified time points before and after surgery.

Main study parameters/endpoints: The difference in early post-operative and long term inflammatory response between EVAS and EVAR, measured by the incidence of the post-implant syndrome. To investigate the incidence of the post-implant syndrome, the rise in CRP, WBC and circulating cytokines, at specified time points up to 12 months after surgery and the change in aortic thrombus volume and its relationship with the inflammatory response, measured by cytokines' concentrations.

详细描述

Endovascular sealing of abdominal aortic aneurysms (EVAS) is a new technique to treat infrarenal abdominal aortic aneurysms (AAA), which can be performed more expeditiously than endovascular aneurysm repair (EVAR). The difference with EVAR is that fixation and seal are provided from polymer filled endobags that are placed in the aneurysmal sac. The post-implantation syndrome (PIS) is the clinical and biochemical expression of an inflammatory response following endovascular repair of an aortic aneurysm. More specifically, the presence of fever (body temperature >38 C for ≥1 day) and leukocytosis (white blood cell count (WBC) >12.000/mL) with negative blood cultures and is occurring in over 30% cases after EVAR. It is related to prolonged hospital stay and elevated CRP levels, that in turn increase the risk on major adverse cardiac events. The literature showed that the magnitude of the post-operative inflammatory response depends on the type of endoprothesis used for EVAR and that EVAS is related to a lower post-operative CRP level, lower white blood counts, a lower temperature and less cardiac complications compared to standard EVAR.

The current study was designed to explore the occurence of the post-implant syndrome after EVAR and EVAS. This study was also designed to unravel the cytokines which are involved in the post-implant syndrome after EVAR and EVAS.

In this international, prospective, explorative study 60 patients who are scheduled for EVAR and 60 patients who are scheduled for EVAS will be included. Blood samples (for WBC and circulating cytokines (TNF-α, Interleukin (IL)-1, 1RA, 6, 10, 18, CRP), Troponin T, HsTnT, NT-pro-BNP)) will be taken at:

  • Before induction of anesthesia
  • At wound closure
  • 24 hours after surgery
  • 48 hours after surgery
  • 1 month after surgery
  • 6 months after surgery
  • 12 months after surgery

Patients are finished with the study after 12 months of follow-up.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

盲法说明

No masking since patients, doctor and researchers know if patients undergo EVAR or EVAS.

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Elective EVAR/EVAS
  • •Ability and willingness to provide written informed consent
  • •Age >50 years

排除标准

  • •Complex EVAR or EVAS, including iliac branched and supra-renal repairs (pre-planned visceral chimneys, fenestrations or branches)
  • •Ruptured or symptomatic AAA
  • •Planned internal iliac artery embolization
  • •Acute or chronic inflammatory illness (i.e. upper respiratory tract infection)
  • •Active rheumatoid arthritis
  • •Inflammatory bowel disease, etc.)
  • •Inflammatory and mycotic aneurysms
  • •Planned associated surgical procedure (i.e. iliac conduit, femoral endarterectomy, etc.)
  • •Previous aortic surgery (open or endovascular)
  • •Untreated malignancy
  • •Major surgery six weeks before EVAR/EVAS
  • •Ongoing or recent immunosuppressive treatment, including corticosteroid use

研究组 & 干预措施

Endovascular Aneurysm Repair (EVAR)

Other

Patients scheduled for EVAR will be included and blood samples at 7 time points will be taken.

干预措施: Endovascular Aneurysm Repair (EVAR) (Procedure)

Endovascular Aneurysm Sealing (EVAS)

Other

Patients scheduled for EVAS will be included and blood samples at 7 time points will be taken.

干预措施: Endovascular Aneurysm Sealing (EVAS) (Procedure)

结局指标

主要结局

Change in inflammatory response between EVAS and EVAR

时间窗: Up to 12 months after surgery.

The change in early post-operative inflammatory response between EVAS and EVAR, measured by the incidence of the post-implant syndrome.

次要结局

  • Change in aortic thrombus volume(Up to 12 months after surgery.)
  • 30-day Morbidity(Up to 30 days after surgery)
  • Mortality(Up to 12 months after surgery.)
  • Pyrexia post operative(24 to 48 hours after surgery)
  • 1 year morbidity(Up to 12 months after surgery.)
  • Cardiac complications(Up to 12 months after surgery.)

研究者

发起方
Rijnstate Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michel Reijnen

Principal investigator

Rijnstate Hospital

研究点 (7)

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