484 Participants NeededMy employer runs this trial

Personalized Thromboprophylaxis for Peripheral Artery Disease

Recruiting at 1 trial location
SB
AD
Overseen ByAnahita Dua, MBCHB, MBA, MSC
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Massachusetts General Hospital
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial investigates whether a personalized approach to preventing blood clots is more effective than the standard method for individuals with peripheral artery disease (PAD) who have undergone surgery to improve leg blood flow. It evaluates whether the personalized plan can better reduce blood clots, amputations, repeat surgeries, bleeding, and death compared to usual treatments. Participants will join either a personalized treatment group, where medication is adjusted based on blood tests, or a standard treatment group. Individuals who have had a procedure to restore blood flow in their legs due to PAD and are experiencing PAD-related issues might be suitable candidates for this trial. As an unphased trial, this study provides a unique opportunity to explore innovative treatments that could enhance health outcomes.

Do I have to stop taking my current medications for the trial?

The trial information does not specify if you need to stop your current medications. However, since the trial involves adjusting medications based on blood test results, it's possible that changes to your medication regimen might be required.

What prior data suggests that this personalized thromboprophylaxis plan is safe for adults with peripheral artery disease?

Previous studies have used a test called thromboelastography with platelet mapping (TEG-PM) to tailor treatment for people with peripheral artery disease (PAD). This test helps doctors assess blood clotting to adjust medications and lower the risk of blood clots. Research has shown that TEG-PM can predict clotting risks and guide the safer use of blood-thinning treatments.

The trial involves medications like aspirin, clopidogrel, rivaroxaban, and ticagrelor, which are common blood thinners. These medications are usually well-tolerated, but they can have side effects. The most common side effect is bleeding, although serious bleeding is rare.

Overall, using TEG-PM to guide these medications aims to enhance safety by customizing treatment to each person's needs.12345

Why are researchers excited about this trial?

Researchers are excited about this trial because it's exploring a personalized approach to preventing blood clots in people with Peripheral Artery Disease (PAD). Unlike the standard treatment, which typically follows a one-size-fits-all protocol, this approach uses Thromboelastography with Platelet Mapping (TEG-PM) to guide therapy. By adjusting medication based on real-time platelet activity, the goal is to keep blood clot prevention within a safe range, potentially improving outcomes and reducing side effects. This tailored strategy could lead to more effective and safer management of PAD compared to current methods.

What evidence suggests that this trial's treatments could be effective for peripheral artery disease?

Research has shown that thromboelastography with platelet mapping (TEG-PM) can help customize treatment for patients with peripheral artery disease (PAD) and predict their health outcomes. In this trial, participants in the TARGET arm will have their antiplatelet therapy adjusted based on TEG-PM results to maintain platelet inhibition within a therapeutic window. Even with standard treatment, up to 17% of patients develop blood clots within six months after procedures to improve blood flow. TEG-PM provides a detailed, personalized view of blood clot formation, enabling doctors to adjust treatments. Studies have found that 60-65% of patients do not fully respond to standard antiplatelet therapy, suggesting that a personalized approach could lead to better results. This method aims to prevent excessive platelet clumping, reducing the risk of clots, repeat procedures, and other complications.12346

Are You a Good Fit for This Trial?

This trial is for adults with peripheral artery disease who have had a procedure to restore blood flow to their legs. Participants must be able to take blood-thinning medications and undergo regular blood tests.

Inclusion Criteria

I have had a major artery injury or surgery to restore blood flow in my limb.
I am 18 years old or older.

Exclusion Criteria

I am currently pregnant.
I have severe liver problems.
I am younger than 18 years old.
See 4 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either the personalized TARGET plan or standard treatment with antiplatelet therapy, with regimen adjustments guided by TEG-PM assessments in the TARGET group.

12 months
Visits at 1 week, 1, 3, 6, 9, and 12 months post-procedure

Follow-up

Participants are monitored for safety and effectiveness, including assessments of arterial thrombosis, platelet inhibition levels, clopidogrel resistance, Rutherford score, and wound status.

12 months
Follow-up visits coincide with treatment phase visits

Open-label extension (optional)

Participants may continue to receive the study drug beyond the initial 12-month period if deemed beneficial.

Long-term

What Are the Treatments Tested in This Trial?

Interventions

  • Aspirin
  • Clopidogrel
  • Rivaroxaban
  • Thromboelastography with Platelet Mapping
  • Ticagrelor

Trial Overview

The study compares a personalized plan (using blood tests to adjust anti-clotting medication like aspirin, rivaroxaban, ticagrelor, or clopidogrel) versus standard treatment after leg procedures. Participants are randomly assigned to either group.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: TARGETExperimental Treatment5 Interventions
Group II: Standard of Care (SOC)Active Control5 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Massachusetts General Hospital

Lead Sponsor

Trials
3,066
Recruited
13,430,000+

Citations

Thromboelastography and clinical outcomes in peripheral ...

TEG-PM could serve as a valuable tool for tailoring antiplatelet therapy and predicting outcomes in patients with PAD.

Platelet function testing and clinical outcomes in peripheral ...

Studies that examined PFT outcomes in patients with PAD after lower extremity revascularization were included. Results. Ten studies met the inclusion criteria.

Thromboelastography With Platelet Mapping to Guide ...

Despite standard antiplatelet therapy, thrombosis occurs in up to 17% of patients within 6 months of revascularization. 60-65% of patients exhibit partial or ...

Peripheral Arterial Disease (PAD) The Use of Clot Strength ...

Thromboelastography with platelet mapping (TEG-PM) leverages dual-pathway metrics to provide comprehensive, individualized coagulation profiles. This method ...

Thromboelastography With Platelet Mapping to Guide ...

The goal of this clinical trial is to learn if a blood clotting test called thromboelastography with platelet mapping (TEG-PM) can guide blood-thinning ...

Thromboelastography to Support Clinical Decision Making ...

Thromboelastography is a rapid and simple way to evaluate a patient's coagulation status and to assess for abnormalities in platelet function and fibrinolysis ...