New device for leg clots tested in first human survey
NCT ID NCT07335341
First seen Jun 27, 2026 · Last updated Aug 12, 2026 · Updated 4 times
Summary
This study surveys doctors who use the Liberant system to remove fresh blood clots from leg arteries and veins. About 50 patients aged 22 or older will be treated within 72 hours of their procedure. The goal is to confirm the device is safe and works as intended.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for ACUTE DVT OF LOWER EXTREMITY are added.
By submitting, you agree to our Terms of use
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
-
Baylor Heart Hospital Of Plano
RECRUITINGPlano, Texas, 75093, United States
-
MedStar Health
RECRUITINGWashington D.C., District of Columbia, 003329, United States
-
Mount Sinai
RECRUITINGNew York, New York, 10029, United States
-
Naples Comprehensive Health
RECRUITINGNaples, Florida, 34108, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Beetroot juice may boost heart blood flow and walking in leg artery disease
- Can a Pre-Surgery skin coating stop wound infections?
- Can a 'Scoring' balloon unclog leg arteries better and reduce stents?
- Can a temporary stent keep leg arteries open?
- Can a Lab-Grown artery graft outlast current options?
- Can a phone app replace cardiac rehab? a new trial puts digital heart care to the test