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IschemiaPhase 1/2CVAALRNCT04168398

Clopidogrel Aspirin Therapy (CAT) Versus Apixiban Aspirin Therapy (AAT) After Lower Limb Revascularization

A Phase 1/2 study testing Combination drug in people with Ischemia and Anticoagulants, run by Mansoura University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

the Aim of the work is to compare the effect of CAT (Clopidogrel aspirin therapy) and AAT (Apixiban aspirin therapy) after lower extremity revascularization. The study will be conducted at the department of vascular surgery in Mansoura university hospitals in a randomized controlled Prospective study over 2 years… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Ischemia, Anticoagulants
What is being tested?
Combination drug
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,536 participants
Where
1 siteEgypt
Study dates
3 Jul 2019to 3 Nov 2021
Phase
Phase 1/2
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 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Symptomatic peripheral artery disease according to Rutherford stages 3 to 6.

Who cannot join

  • Patients with severe groin or limb infection.
  • who can't give consent (unconscious)
  • Those with mental or behavioral disorders will be excluded.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Mansoura

    Al Mansurah, Mansoura University, 35111

Other trials in Egypt

About this study

the Aim of the work is to compare the effect of CAT (Clopidogrel aspirin therapy) and AAT (Apixiban aspirin therapy) after lower extremity revascularization.

The study will be conducted at the department of vascular surgery in Mansoura university hospitals in a randomized controlled Prospective study over 2 years: 2019-2021. It will include all patients presented to our department fulfilling the ,We revascularize about 5-10 limbs per week and the study will be carried over 30 months; sample size will be 600-1200 patients,The study will be conducted in patients with lower limb ischemia who need revascularization. All Symptomatic peripheral artery disease according to Rutherford stages 3 to 6; will be included Patients with severe groin or limb infection, can't give consent (unconscious) and those with mental or behavioral disorders; will be excluded.

Therapies:CAT (Clopidogrel aspirin therapy) Clopidogrel 75 mg (Plavix 75mg) plus Aspirin 81 mg. AAT (Apixiban aspirin therapy): Apixiban 2.5 twice daily (Eliquis 2.5mg) plus Aspirin 81 mg. Every patient will be followed every week till first month, then every 3 months till 1 years. Hemodynamic improvement was assessed by ankle brachial pressure index (ABI), performed before and after the procedure and every 3 months. Evaluation made by CTA or duplex ultrasonography to determine 1ry and 2ry patency, Coagulation profile (platelet count, INR, prothrombin time and activated partial thromboplastin time). Adverse bleeding complications will be documented

Read the detailed description

INTRODUCTION:

Atherothrombotic disorders of the cerebrovascular, coronary, and peripheral arterial circulation, affect nearly 20-30% of those older than 70 years of age and are among the leading causes of death and disability in the world. Individuals with peripheral artery disease (PAD), referring to arterial vascular disease of the extremities, have the greatest risk of experiencing cardiovascular death and myocardial infarction when compared to those with coronary artery disease or cerebrovascular disease alone PAD usually signals more systemic atherosclerotic disease and often goes undiagnosed and undertreated, which is thought to be a major reason for why these patients have been found to be at increased risk for major adverse cardiovascular events and mortality. One of the major goals of antiplatelet therapy is for prevention, both primary and secondary, of acute thrombotic events. Despite the increased local and systemic cardiovascular risk in PAD patients, the literature on the most effective antiplatelet regimen and its recommended duration are lacking, especially compared to studies primarily focusing on coronary artery disease. The major consensus guidelines for PAD suggest using mono antiplatelet therapy in PAD but state that the data either for or against the use of DAPT in this population are too limited to make strong recommendations. There has been an attempt to update the international TASC guidelines but disagreement among the societies has delayed a universally accepted TASC III document. After PAD revascularization, corresponding risks are even higher, with reported rates of nonfatal MI, ischemic stroke, or cardiovascular death 36 months after procedure of 14% among patients with IC and 34% among those with CLI. These risks are further elevated after repeat limb revascularization, supporting the need for more aggressive secondary prevention measures, including intensive antithrombotic therapy, to prevent recurrent events in this high-risk population. Despite the greater risk of cardiovascular and limb adverse outcomes in patients with PAD undergoing limb revascularization, high-quality data on antithrombotic therapy in this clinical context are sparse. As a result, recommendations regarding antithrombotic therapy for these patients are based on lower levels of evidence and are inconsistent.

Until now no clinical trial had reported the use of AAT (Apixiban aspirin therapy) after lower limb revascularization therefore, the purpose of this study is to evaluate and compare the effect of CAT (Clopidogrel aspirin therapy) and AAT (Apixiban aspirin therapy) at time of discharge, on survival following lower extremity revascularization and major adverse effects Aim of the work compare the effect of CAT (Clopidogrel aspirin therapy) and AAT (Apixiban aspirin therapy) after lower extremity revascularization.

Outcome Primary outcomes: Major adverse limb events (MALES);

  • Endovascular or surgical revascularization
  • Acute vessel thrombosis,
  • Amputation of the target limb Secondary outcomes: Major adverse cardiovascular events (MACE);
  • Nonfatal stroke
  • Nonfatal myocardial infarction
  • Cardiovascular death. Patients and methods Study location: The study will be conducted at the department of vascular surgery in Mansoura university hospitals Type of study: Randomized controlled Prospective study Study duration: 2 years: 2019-2021 Sample size: It will include all patients presented to our department fulfilling the inclusion criteria. We revascularize about 5-10 limbs per week and the study will be carried over 30 months; sample size will be 600-1200 patients Study population: The study will be conducted in patients with lower limb ischemia who need revascularization.

Inclusion criteria: Symptomatic peripheral artery disease according to Rutherford stages 3 to 6.

Exclusion criteria

  1. Patients with severe groin or limb infection.
  2. who can't give consent (unconscious)
  3. Those with mental or behavioral disorders will be excluded. Consent: Patients after signing informed consent that possible complication from the procedure ought to happen and what are the alternatives.

Data collection: The demographics, Symptoms and preoperative clinical data will be collected History Data: included patient's demographics, underlying medical conditions, any previous associated morbidity.

Examination: Arterial assessments. Laboratory: Blood picture, Blood sugar level, Kidney functions, Liver functions and Coagulation profile.

Imaging: Duplex US and CTA Method of Randomization: Block randomization: Two elements A for CAT, B for AAT A A B B A B A B A B B A B B A A B A B A B A A B Therapies CAT (Clopidogrel aspirin therapy) Clopidogrel 75 mg (Plavix 75mg) plus Aspirin 81 mg.

AAT (Apixiban aspirin therapy):

Apixiban 2.5 twice daily (Eliquis 2.5mg) plus Aspirin 81 mg. Follow up

  • Every patient will be followed every week till first month, then every 3 months till 1 years.
  • Hemodynamic improvement was assessed by ankle brachial pressure index (ABI), performed before and after the procedure and every 3 months.
  • Evaluation made by CTA or duplex ultrasonography to determine 1ry and 2ry patency
  • Coagulation profile (platelet count, INR, prothrombin time and activated partial thromboplastin time).
  • Adverse bleeding complications.
  • Both MACEs and MALEs will be documented Statistical analysis
  • The data will be analyzed using Statistical Package for the Social Sciences. The numerical outcomes e.g. age is calculated as mean. Gender will be recorded as frequency and percentage. Chi Square test is applied to assess the association of various parameters. The results will be considered statistically significant if the p-value is found to be less than or equal to 0.05.
Being tested
Combination drug
Keywords
Clopidogrel, Apixiban and Lower Limb Revascularization
Medical subject headings
Ischemia

What participants receive

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

  • Combination drugDrug

    Also called anticoagulations plus antiplatelets

    Anticoagulation

Study groups in NCT04168398
Study groupRoleWhat they receive
Plavix 75mg and juspirin 81 mg therapyExperimentalClopidogrel 75 mg (Plavix 75mg) plus Aspirin (juspirin) 81 mg.
Receives: Drug: Combination drug
Eliquis 2.5mg and juspirin 81 mg therapy):ExperimentalApixiban 2.5 twice daily (Eliquis 2.5mg) plus Aspirin (juspirin) 81 mg.
Receives: Drug: Combination drug

What is being measured

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

  1. Major adverse limb events (MALES);

    • Endovascular or surgical revascularization
    • Acute vessel thrombosis,
    • Amputation of the target limb

    Measured: two year

Secondary outcomes (1)
  1. Major adverse cardiovascular events (MACE);

    • Nonfatal stroke
    • Nonfatal myocardial infarction
    • Cardiovascular death.

    Measured: two year

Timeline

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

  1. First posted19 Nov 2019
  2. Study start3 Jul 2019
  3. Primary completion1 Nov 2021
  4. Study completion3 Nov 2021

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 1/2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized controlled Prospective study: It will include all patients presented to our department fulfilling the inclusion criteria. We revascularize about 5-10 limbs per week and the study will be carried over 30 months; sample size will be 600-1200 patients
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
1,536 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04168398
Sponsor's protocol ID
R.19.06.544.R1 - 2019/07/03
Acronym
CVAALR
Status last verified
Jul 2022
First submitted
25 Oct 2019
Last updated
19 Jul 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided: The demographics, Symptoms and preoperative clinical data will be collected History Data: included patient's demographics, underlying medical conditions, any previous associated morbidity. Examination: Arterial assessments. Laboratory: Blood picture, Blood sugar level, Kidney functions, Liver functions and Coagulation profile.

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Combination drug in people with Ischemia and Anticoagulants, run by Mansoura University at 1 site in Egypt.

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 1 inclusion and 3 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: finished, as of the sponsor's last update on 19 Jul 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. 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 combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

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

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Major adverse limb events (MALES); (time frame: two year). 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 19 Jul 2022.

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