AzTrials
AzTrials

Peripheral Arterial DiseasePhase 4TRAIANONCT01627431

Residual Platelet Activity In Advanced Peripheral Artery Disease

A Phase 4 study testing Acetylsalicylic acid and Clopidogrel in people with Peripheral Arterial Disease, run by University of Roma La Sapienza at 2 sites in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

The peripheral arterial disease (PAD) is a common atherosclerotic disease manifestation and its prevalence increase with age and with the simultaneous presence of cardiovascular risk factors. Read more about this study

Who is it for?
Ages 40 to 80 years
Conditions the study is for
Peripheral Arterial Disease
What is being tested?
Acetylsalicylic acid and Clopidogrel
Could I receive a placebo?
No, everyone receives an active treatment
How many people
410 participants
Where
2 sitesItaly
Study dates
Jul 2012to Jul 2015
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Claudicatio Intermittens affected patients in which both exercise than pharmacological therapies failed
  • Ankle Brachial Index < 0.9 or > 1.3
  • Peripheral Arteries stenosis > 50% bilateral

Who cannot join

  • Acute Limb Ischemia patients
  • Patients that underwent a peripheral revascularization procedure within 6 months

Trial locations and contacts

2 sites in 1 country.

Francesco Violi, Prof contact

+39-06-4461933

francesco.violi@uniroma1.it

Stefania Basili, Prof contact

+39-06-49974678

stefania.basili@uniroma1.it

Italy2 sites, 2 recruiting
  • University of Florence - Azienda Ospedaliero-Universitaria Careggi

    Florence, Florence, 50134

    Rosanna Abbate, MD, 055 7949417 ext. +39, rosanna.abbate@unifi.it

    Rosanna Abbate, MD

    Not yet recruiting
  • Sapienza- University of Rome -Azienda Policlinico Umberto I

    Rome, Rome, 00161

    Francesco Violi, MD, 06 4461933 ext. +39, francesco.violi@uniroma1.it

    Stefania Basili, MD, 06 49974678 ext. +39, stefania.basili@uniroma1.it

    Recruiting

Other trials in Italy

About this study

Official title: Tailored Strategy for Residual Platelet Activity In Advanced Peripheral Artery Disease: New Optimal Management.

The peripheral arterial disease (PAD) is a common atherosclerotic disease manifestation and its prevalence increase with age and with the simultaneous presence of cardiovascular risk factors.

PAD patients are usually treated, as a first line treatment, with the exercise therapy, combined with the pharmacological antiplatelet therapy.

Read more

In the case of first line therapy failure, PAD patients usually undergoing to invasive revascularization procedures.

After a peripheral stent has been located, the major follow-up problem is the restenosis rate.

Published studies describe how, in a large amount of patients, can be recognised an high residual platelet activity. These data about PAD patients at the moment are lacking .

The authors would evaluate the incidence of PAD patients with an high residual platelet activity.

Read the detailed description

The peripheral arterial disease (PAD) is a common atherosclerotic disease manifestation and its prevalence increases with age and with the co-presence of cardiovascular risk factors. PAD affects a large proportion of the adult population, with an age-adjusted prevalence of 4-15% which increases to 29% in case of comorbidity such as the presence of diabetes mellitus in the same individual. Less than 20% of patients with peripheral arterial laments the typical symptom of "claudication intermittens". Studies on the symptomatic PAD natural history indicate that the risk of limb loss in non-diabetic patients is low (2% or less), but the cardiovascular disease represent the leading cause of death; the annual rate of cardiovascular events (myocardial infarction, stroke or cardiovascular death) is between 5 and 7%. Medical treatment and / or surgery in this type of patient should be directed not only to improve the walking autonomy but also to reduce cardiovascular risk. Claudicant patients first-line therapy is based on structured physical exercise program and, in some specific cases, on the antiplatelet pharmacological therapy. The lack of response to exercise and / or drug therapy should lead to the next level of decision making, which is to consider limb revascularization procedures. However, in patients with suspected proximal lesion (gluteal claudication or absent femoral pulse), revascularization procedures could be considered as a first line therapy. When the revascularization procedures are considered, the first choice intervention should be the endovascular strategy, considering the lowest number of periprocedural complications. Recommendations for optimal drug therapy after revascularisation procedures in the lower limbs are hampered by lack of agreement on the optimal role of these procedures, and lack of data from randomized clinical trials. Transluminal angioplasty (PTA), primary or associated with stenting, is recommended for focal stenotic lesions of the iliac (common and external first section) and femoral-popliteal axis, particularly when the claudication intermittents is considered as severe, rather than critical ischemia. Also, this approach is recommended in non-diabetic patients with a relatively preserved tibial vessels flow. Exists a minor agreement about endovascular procedures use in extended occlusive lesions. In recent years, has become more common the use of open or covered stents during endovascular treatments in order to make it more secure and durable over time, especially in obstructive and extended lesions. This has certainly led to improved primary patency outcomes, but has entailed and still entails additional problems of drug therapy agreement.

Nowadays, the main problem concerning lower limbs revascularization is the post-procedure anti-thrombotic pharmacological treatment and the different antiplatelet drugs effectiveness This issue was addressed in two meta-analyses, where have been shown how the data are not conclusive. Moreover, a recent study by Marcucci et al (Circulation. 2009; 119: 237-42) has clearly shown that impaired platelet activation inhibition is a crucial point for the prevention of vascular outcomes, because residual platelet reactivity has been associated with adverse vascular outcomes.

Overall, these data identify two key issues:

  1. Platelet hyperactivation, usually observed after revascularization procedures;
  2. The platelet inhibition percentage appears crucial to reduce postoperative thrombotic complications and restenosis early onset.

Therefore, a unique aspect of this study is to analyze whether after peripheral revascularization procedures a platelet hyperactivation is observed and evaluate the possible involved mechanisms. In fact, the knowledge of the underlying mechanism could lead to more appropriate pharmacological approach to prevent platelet activation. In this context, the authors would explore the role of reactive oxygen species (ROS) in inducing platelet activation in patients with PAD undergoing revascularization devices.

Being tested
Acetylsalicylic acid, Clopidogrel
Keywords
PAD, Peripheral revascularization, Antiplatelet therapy, Residual platelet activity
Medical subject headings
Peripheral Arterial Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Acetylsalicylic acidDrug

    Also called Aspirin

    100 mg once per day

  • ClopidogrelDrug

    Also called Plavix

    75 mg once per day

Study groups in NCT01627431
Study groupRoleWhat they receive
Antiplatelet therapyOtherPatients underwent peripheral revascularization procedures undergoing a double antiplatelet therapy
Receives: Drug: Acetylsalicylic acid; Drug: Clopidogrel

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Residual Platelet Activity

    Evaluate the high residual platelet activity prevalence in PAD patients

    Measured: 2 years

Secondary outcomes (6)
  1. Target vessels thrombosis

    Evaluate the target vessels thrombosis incidence

    Measured: 2 years

  2. Major Cardiac Events

    Evaluate the Major Cardiac Events (MACE) incidence in PAD patients undergoing the peripheral revascularization procedures.

    Measured: 2 years

  3. Platelet aggregation tests

    Compare the different platelet aggregation tests specificity, sensitivity, accuracy and predictive values

    Measured: 2 years

  4. Oxidative stress

    Evaluate platelet activation and oxidative stress indexes relationship

    Measured: 2 years

  5. Laboratory tests predictive values

    Evaluate the different laboratory tests (platelet aggregation, oxidative stress markers, seric thromboxane) predictive values in identify recurrent thrombosis high risk patients

    Measured: 2 years

  6. High risk patients score

    Validate a clinical-laboratoristic predictive score in order to identify recurrent thrombosis high risk patients

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jun 2012 (estimated)
  2. Study startJul 2012
  3. Primary completionJul 2014 (estimated)
  4. Study completionJul 2015 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
410 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01627431
Sponsor's protocol ID
SAPIENZA-PAD
Acronym
TRAIANO
Status last verified
Nov 2012
First submitted
14 Jun 2012
Last updated
28 Nov 2012
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Acetylsalicylic acid and Clopidogrel in people with Peripheral Arterial Disease, run by University of Roma La Sapienza at 2 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 28 Nov 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Francesco Violi, Prof (+39-06-4461933, francesco.violi@uniroma1.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Residual Platelet Activity (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Nov 2012.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in