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Completed

NCT Number: NCT01943591

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Foothills Medical Center, Calgary, Alberta, Canada

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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)

Exclusion criteria

  • 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

Treatment and study plan

Endovascular coiling with standard 10-caliber platinum coils or 15-caliber platinum coils

Device

Embolization using 15-caliber platinum coils or standard 10-caliber platinum coils.

Primary outcomes

  1. Major Recurrence of Lesion or Presence of Residual Aneurysm

    Time frame: 1 year

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

  2. Hemorrhage During the Follow-up Period

    Time frame: Within 1 year following coiling

    Post-treatment hemorrhage experienced during follow-up period.

  3. Retreatment of the Same Lesion by Endovascular or Surgical Means

    Time frame: Within 1 year following coiling

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

  4. Initial Treatment Failure

    Time frame: Within 1 year following coiling

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

  5. Related Morbidity

    Time frame: Within 1 year following coiling

    Morbidity that precludes follow up

  6. Related Mortality

    Time frame: Within 1 year following coiling

    Mortality that precludes follow up

Secondary outcomes

  1. Packing Density

    Time frame: within the first 3 days after coiling

    Packing density with the number of coils implanted

  2. Procedural Serious Adverse Events (SAEs)

    Time frame: Within 6 months following coiling

    Procedural-related serious adverse events

  3. Modified Rankin Score (mRS) Greater Than 2

    Time frame: at 1 year follow-up

    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).

Sponsors and collaborators

Lead sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Other

Collaborators

  • DePuy Synthes
  • Johnson & Johnson Medical Companies

Registry information

Acronym: DELTA

Important dates

Study start
2013
Primary completion
2018
Study completion
2018
First posted
Sep 17, 2013
Registry last updated
Jan 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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