🔎 Trials Near Me

Home › Ischemic Stroke › NCT07491952

Continuous Dual Aspiration Technique With Zoom System for Stroke

RecruitingObservational study

Clinical Evaluation of Continuous Dual Aspiration Technique With Zoom System for Stroke (ADAPT 2.0)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Subject is ≥ 18 years of age
2. Subject or legally authorized representative has provided written informed consent prior to any study-specific procedures and no later than 72 hours after the index procedure
3. Pre-stroke mRS 0-2
4. Subject is undergoing or has undergone an aspiration thrombectomy using the Zoom System with Continuous Dual Aspiration Technique (CDAT) as the first line device within its intended use

Exclusion Criteria:

1. Subjects with a life expectancy of less than 6 months
2. Female subject who is known to be pregnant at time of admission
3. Any intracranial hemorrhage in the qualifying head CT or MRI
4. Presence of tandem internal carotid artery occlusion, multiple occlusion locations (e.g., cavernous ICA and M1, separate M2 occlusions, etc.), or occlusions in multiple territories (e.g., MCA and ACA, bilateral, etc.).
5. In the opinion of the Investigator, the patient is not a suitable candidate for intervention with the Zoom System
6. Subject is currently enrolled in or planned to be enrolled in any concurrent interventional study that may impact the safety or performance data collected in this study

About the study

This study is designed to evaluate the effectiveness, safety and clinical performance of ADAPT 2.0, first-line aspiration neurothrombectomy with Zoom System with Continuous Dual Aspiration Technique (CDAT).

What is being tested

Sponsor: Imperative Care, Inc. · Participants: 750 · Started: Mar 24, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07491952

Locations in the U.S.

AlabamaHuntsville Hospital, Huntsville
CaliforniaJohn Muir Health, Walnut Creek
FloridaUniversity of South Florida, Tampa
GeorgiaWellstar Kennestone Hospital, Marietta
LouisianaOchsner Clinic Foundation (Lafayette), Lafayette
Ochsner Clinic Foundation, New Orleans
MarylandUniversity of Maryland, Baltimore
MinnesotaAllina Health, Minneapolis
New YorkAlbany Medical College, Albany
University at Buffalo Neurosurgery, Buffalo
Icahn School of Medicine at Mount Sinai, New York
Montefiore Medical Center, The Bronx
OklahomaUniversity of Oklahoma, Health Science Center, Oklahoma City
South CarolinaPrisma Health - Upstate, Greenville
TennesseeFort Sanders Regional Medical Center, Knoxville
Semmes Murphey Foundation, Memphis
TexasHCA Houston Healthcare Kingwood, Kingwood
Methodist Healthcare System of San Antonio, San Antonio
University of Texas Science Health Center at San Antonio, San Antonio
UtahUniversity of Utah, Salt Lake City
VirginiaInova Fairfax Medical Campus, Falls Church
WashingtonProvidence Sacred Heart Medical Center and Children's Hospital, Spokane

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.