跳至主要内容
临床试验/NCT01943591
NCT01943591已完成不适用

DELTA Trial: Does Embolization With Larger Coils Lead to Better Treatment of Aneurysms Trial

Centre hospitalier de l'Université de Montréal (CHUM)15 个研究点 分布在 2 个国家目标入组 210 人开始时间: 2013年11月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
210
试验地点
15
主要终点
Related Morbidity

研究概览

简要总结

Endovascular treatment with platinum coils is safe and effective in preventing rebleeding of intracranial aneurysms. Unfortunately, endovascular treatment of aneurysms with coils has been associated with incomplete occlusion at initial treatment (remnant) or at follow-up (recurrence). This in some studies has been as high as 20%. While many such aneurysm remnants or recurrences exhibit benign behavior, many require retreatment to prevent future hemorrhage.

A recent randomized controlled trial of aneurysm coiling revealed that aneurysms between 2 and 9.9 mm diameter were more likely to have an improved angiographic and composite clinical outcome when treated with hydrogel-coated coils, an improvement inferred to result from higher packing density afforded by hydrogel expansion(1). The use of hydrogel coils is associated with technical difficulties related to expansion and limited time for deployment. The investigators theorize that similar results could be achieved by using more voluminous bare platinum coils, leading to improved packing density compared to smaller caliber coils, and thus result in lower incidence of remnants or residuals. The relationship between packing densities and composite clinical endpoints having never been shown in a robust fashion, the investigators therefore propose a randomized clinical trial opposing coiling with soft 15-caliber coils to 10-caliber bare platinum coils in aneurysms varying in size from 3 to 9.9 mm.

To test the hypothesis that 15-caliber coiling systems are superior to standard 10-caliber coils in achieving better composite outcomes, the investigators propose the DELTA trial: Does Embolization with Larger coils lead to better Treatment of Aneurysms trial, a randomized controlled blinded trial with 2 subgroups of 282 patients each, 564 total:

Subgroup 1: Coiled with a maximum proportion of 15-caliber coils as conditions allow Subgroup 2: Coiled with 10-caliber coils.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •At least one ruptured or unruptured aneurysms with a dimension ≥ 10 mm (longest axis)
  • •for ruptured lesions, patients should be in World Federation of Neurosurgical Societies (WFNS) grade < IV.
  • •The anatomy of the lesion is such that endovascular treatment is possible with both types of coils (not necessarily certain or probable)
  • •Patient is 18 or older
  • •Life expectancy is more than 2 years (able to complete follow-up)

排除标准

  • •Patients with planned treatment of an associated cerebral arteriovenous malformations
  • •When parent vessel occlusion, without simultaneous endosaccular coiling of the aneurysm, is the primary intent of the procedure
  • •Any absolute contraindication to endovascular treatment, angiography, or anaesthesia such as severe allergies to contrast or medications

研究组 & 干预措施

15-caliber platinum coils

Experimental

Endovascular embolization coiling using 15-caliber platinum coils

干预措施: Endovascular coiling with standard 10-caliber platinum coils or 15-caliber platinum coils (Device)

10-caliber coils

Active Comparator

Endovascular embolization coiling using standard 10-caliber platinum coils

干预措施: Endovascular coiling with standard 10-caliber platinum coils or 15-caliber platinum coils (Device)

结局指标

主要结局

Related Morbidity

时间窗: Within 1 year following coiling

Morbidity that precludes follow up

Related Mortality

时间窗: Within 1 year following coiling

Mortality that precludes follow up

Major Recurrence of Lesion or Presence of Residual Aneurysm

时间窗: 1 year

Major radiographic recurrence of the lesion or the presence of a 'residual aneurysm' as judged by core lab

Retreatment of the Same Lesion by Endovascular or Surgical Means

时间窗: Within 1 year following coiling

Retreatment of the same lesion by endovascular or surgical means during the follow-up period

Hemorrhage During the Follow-up Period

时间窗: Within 1 year following coiling

Post-treatment hemorrhage experienced during follow-up period.

Initial Treatment Failure

时间窗: Within 1 year following coiling

Inability to treat aneurysm, either because access to aneurysm is difficult or technical issues.

次要结局

  • Packing Density(within the first 3 days after coiling)
  • Procedural Serious Adverse Events (SAEs)(Within 6 months following coiling)
  • Modified Rankin Score (mRS) Greater Than 2(at 1 year follow-up)

研究者

发起方
Centre hospitalier de l'Université de Montréal (CHUM)
申办方类型
Other
责任方
Sponsor

研究点 (15)

Loading locations...

相似试验