Blood test may prevent clots after leg surgery
NCT ID NCT07597239
First seen Jun 27, 2026 · Last updated Sep 09, 2026 · Updated 5 times
Summary
This study looks at whether a special blood test (TEG-PM) can guide doctors in adjusting blood-thinning medications for people who have had leg artery surgery for peripheral artery disease. About 130 adults will have their blood tested before and up to 9 months after surgery, and their medications (aspirin, clopidogrel, or ticagrelor) may be changed based on the results. The goal is to reduce the risk of dangerous blood clots forming in the treated leg.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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514 people
The number who actually took part.
- Started
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Nov 2020
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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60 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients requiring infrainguinal endovascular revascularization for peripheral atherosclerosis * Patients of age 60 or older Exclusion Criteria: * Planned open surgical revascularization (bypass grafting, endarterectomy) * Hybrid procedures involving a significant open surgical component * Contraindication to standard antiplatelet therapy * Pregnancy or breastfeeding * Inability to undergo serial venous blood sampling * Inability to provide informed consent * Technical failure to cross or treat the target lesion via an endovascular approach * Non-atherosclerotic pathology identified as primary etiology
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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
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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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