New stroke device trial halted early – too soon to tell

NCT ID NCT05107206

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a new device called Envi™-SR for removing blood clots in people having a severe ischemic stroke. The goal was to see if it works as well as devices already approved by the FDA. However, the trial was stopped early after enrolling only 12 people, so we don't have enough information to know if the new device is safe or effective.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance
Envi™-SR Thrombectomy device
What this could lead to
If successful, this device could offer another option for quickly removing blood clots in stroke patients, potentially improving recovery.
What could go wrong
The trial was terminated early with only 12 participants, so we have very little data. It is unclear if the device is safe or effective compared to existing tools.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Advocate Aurora Health

    Downers Grove, Illinois, 60068, United States

  • Baptist Health Research Institute

    Jacksonville, Florida, 32207, United States

  • North Shore University Hospital

    Manhasset, New York, 11030, United States

  • Providence Medical Foundation

    Irvine, California, 92612, United States

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