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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
210
Embolization using 15-caliber platinum coils or standard 10-caliber platinum coils.
University of Illinois at Chicago
Chicago, Illinois, United States
University of Massachusetts Medical School
Worcester, Massachusetts, United States
Stony Brook University Medical Center (SUNY)
Stony Brook, New York, United States
SUNY Upstate Medical University
Syracuse, New York, United States
Medical University of South Carolina
Charleston, South Carolina, United States
University of Tennessee Medical Center
Knoxville, Tennessee, United States
University of Virginia Health System
Charlottesville, Virginia, United States
West Virginia University Hospital
Morgantown, West Virginia, United States
Foothills Medical Center
Calgary, Alberta, Canada
University of Alberta Hospital
Edmonton, Alberta, Canada
...and 5 more locations
Major Recurrence of Lesion or Presence of Residual Aneurysm
Major radiographic recurrence of the lesion or the presence of a 'residual aneurysm' as judged by core lab
Time frame: 1 year
Hemorrhage During the Follow-up Period
Post-treatment hemorrhage experienced during follow-up period.
Time frame: Within 1 year following coiling
Retreatment of the Same Lesion by Endovascular or Surgical Means
Retreatment of the same lesion by endovascular or surgical means during the follow-up period
Time frame: Within 1 year following coiling
Initial Treatment Failure
Inability to treat aneurysm, either because access to aneurysm is difficult or technical issues.
Time frame: Within 1 year following coiling
Related Morbidity
Morbidity that precludes follow up
Time frame: Within 1 year following coiling
Related Mortality
Mortality that precludes follow up
Time frame: Within 1 year following coiling
Packing Density
Packing density with the number of coils implanted
Time frame: within the first 3 days after coiling
Procedural Serious Adverse Events (SAEs)
Procedural-related serious adverse events
Time frame: Within 6 months following coiling
Modified Rankin Score (mRS) Greater Than 2
Modified Rankin Score (mRS) that is greater than 2 at 1 year follow-up (or at last follow-up, if applicable). Minimum = 0 (no symptoms), maximum = 6 (Deceased).
Time frame: at 1 year follow-up
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