Continuous Aspiration Technique for Ischemic Stroke

Continuous Dual Aspiration Technique With Zoom System for Stroke

Recruiting Observational Study
Ischemic Stroke Acute Stroke
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
750 (estimated)
Sponsor
Imperative Care, Inc. · Industry
Who this trial is looking for

This trial is looking for adults who have had an ischemic stroke. Participants will undergo a specific type of thrombectomy procedure using a new technique.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old
  • I can provide signed consent for this study
  • My pre-stroke score on the mRS was 0-2
  • I am having or have had a thrombectomy using the Zoom System

You may not be able to join if

  • I have a life expectancy of less than 6 months
  • I am pregnant
  • I have any bleeding in my brain from a recent scan
  • I have multiple blood clots in different areas of my brain
  • My doctor thinks I'm not suitable for this procedure
  • I am taking part in another similar study

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

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).

Trial Locations
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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 as…
Contacts

Pojai Phattanagosai

650-740-7703

pphattanagosai@Imperativecare.com

CONTACT

Emma Pham

408-421-7684

epham@imperativecare.com

CONTACT