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

Primary Purpose

Cerebral Aneurysm

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Endovascular coiling with standard 10-caliber platinum coils or 15-caliber platinum coils
Sponsored by
Centre hospitalier de l'Université de Montréal (CHUM)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Aneurysm focused on measuring treatment trial, cerebral aneurysm, randomized, coils, endovascular, Aneurysm, Intracranial Aneurysm, Vascular Diseases, Cardiovascular Diseases, Intracranial Arterial Diseases, Cerebrovascular Disorders, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University of Illinois at Chicago
  • University of Massachusetts Medical School
  • Stony Brook University Medical Center (SUNY)
  • SUNY Upstate Medical University
  • Medical University of South Carolina
  • University of Tennessee Medical Center
  • University of Virginia Health System
  • West Virginia University Hospital
  • Foothills Medical Center
  • University of Alberta Hospital
  • Queen Elizabeth II Health Sciences Centre
  • McMaster University, Hamilton General Hospital
  • Ottawa Hospital
  • Toronto Western Hospital
  • Centre Hospitalier de l'Université de Montréal

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

15-caliber platinum coils

10-caliber coils

Arm Description

Endovascular embolization coiling using 15-caliber platinum coils

Endovascular embolization coiling using standard 10-caliber platinum coils

Outcomes

Primary Outcome Measures

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
Hemorrhage During the Follow-up Period
Post-treatment hemorrhage experienced during follow-up period.
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
Initial Treatment Failure
Inability to treat aneurysm, either because access to aneurysm is difficult or technical issues.
Related Morbidity
Morbidity that precludes follow up
Related Mortality
Mortality that precludes follow up

Secondary Outcome Measures

Packing Density
Packing density with the number of coils implanted
Procedural Serious Adverse Events (SAEs)
Procedural-related serious adverse events
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).

Full Information

First Posted
September 12, 2013
Last Updated
January 9, 2020
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
DePuy Synthes, Johnson & Johnson Medical Companies
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1. Study Identification

Unique Protocol Identification Number
NCT01943591
Brief Title
DELTA Trial: Does Embolization With Larger Coils Lead to Better Treatment of Aneurysms Trial
Acronym
DELTA
Official Title
DELTA Trial: Does Embolization With Larger Coils Lead to Better Treatment of Aneurysms Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
November 13, 2013 (undefined)
Primary Completion Date
December 5, 2018 (Actual)
Study Completion Date
December 5, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
DePuy Synthes, Johnson & Johnson Medical Companies

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Aneurysm
Keywords
treatment trial, cerebral aneurysm, randomized, coils, endovascular, Aneurysm, Intracranial Aneurysm, Vascular Diseases, Cardiovascular Diseases, Intracranial Arterial Diseases, Cerebrovascular Disorders, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
210 (Actual)

8. Arms, Groups, and Interventions

Arm Title
15-caliber platinum coils
Arm Type
Experimental
Arm Description
Endovascular embolization coiling using 15-caliber platinum coils
Arm Title
10-caliber coils
Arm Type
Active Comparator
Arm Description
Endovascular embolization coiling using standard 10-caliber platinum coils
Intervention Type
Device
Intervention Name(s)
Endovascular coiling with standard 10-caliber platinum coils or 15-caliber platinum coils
Intervention Description
Embolization using 15-caliber platinum coils or standard 10-caliber platinum coils.
Primary Outcome Measure Information:
Title
Major Recurrence of Lesion or Presence of Residual Aneurysm
Description
Major radiographic recurrence of the lesion or the presence of a 'residual aneurysm' as judged by core lab
Time Frame
1 year
Title
Hemorrhage During the Follow-up Period
Description
Post-treatment hemorrhage experienced during follow-up period.
Time Frame
Within 1 year following coiling
Title
Retreatment of the Same Lesion by Endovascular or Surgical Means
Description
Retreatment of the same lesion by endovascular or surgical means during the follow-up period
Time Frame
Within 1 year following coiling
Title
Initial Treatment Failure
Description
Inability to treat aneurysm, either because access to aneurysm is difficult or technical issues.
Time Frame
Within 1 year following coiling
Title
Related Morbidity
Description
Morbidity that precludes follow up
Time Frame
Within 1 year following coiling
Title
Related Mortality
Description
Mortality that precludes follow up
Time Frame
Within 1 year following coiling
Secondary Outcome Measure Information:
Title
Packing Density
Description
Packing density with the number of coils implanted
Time Frame
within the first 3 days after coiling
Title
Procedural Serious Adverse Events (SAEs)
Description
Procedural-related serious adverse events
Time Frame
Within 6 months following coiling
Title
Modified Rankin Score (mRS) Greater Than 2
Description
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

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Raymond, MD
Organizational Affiliation
Centre hospitalier de l'Université de Montréal (CHUM)
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Illinois at Chicago
City
Chicago
State/Province
Illinois
Country
United States
Facility Name
University of Massachusetts Medical School
City
Worcester
State/Province
Massachusetts
Country
United States
Facility Name
Stony Brook University Medical Center (SUNY)
City
Stony Brook
State/Province
New York
Country
United States
Facility Name
SUNY Upstate Medical University
City
Syracuse
State/Province
New York
Country
United States
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
Country
United States
Facility Name
University of Tennessee Medical Center
City
Knoxville
State/Province
Tennessee
Country
United States
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
Country
United States
Facility Name
West Virginia University Hospital
City
Morgantown
State/Province
West Virginia
Country
United States
Facility Name
Foothills Medical Center
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 2T9
Country
Canada
Facility Name
University of Alberta Hospital
City
Edmonton
State/Province
Alberta
Country
Canada
Facility Name
Queen Elizabeth II Health Sciences Centre
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 3A7
Country
Canada
Facility Name
McMaster University, Hamilton General Hospital
City
Hamilton
State/Province
Ontario
Country
Canada
Facility Name
Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada
Facility Name
Toronto Western Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 2S8
Country
Canada
Facility Name
Centre Hospitalier de l'Université de Montréal
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H2X 0C1
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
21571149
Citation
White PM, Lewis SC, Gholkar A, Sellar RJ, Nahser H, Cognard C, Forrester L, Wardlaw JM; HELPS trial collaborators. Hydrogel-coated coils versus bare platinum coils for the endovascular treatment of intracranial aneurysms (HELPS): a randomised controlled trial. Lancet. 2011 May 14;377(9778):1655-62. doi: 10.1016/S0140-6736(11)60408-X.
Results Reference
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DELTA Trial: Does Embolization With Larger Coils Lead to Better Treatment of Aneurysms Trial

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