Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07556887

Clinical Impact of Using IMPROVE to Select Patients for Carotid Revascularisation

Narrowing of the carotid artery due to atherosclerosis with an unstable plaque can cause a stroke. Patients with carotid artery disease who have had a TIA or minor stroke and are at high risk of another stroke are often treated with surgery or stenting to remove the plaque. For lower-risk patients, medication alone is the better option, as surgery also carries risks. A new decision method, based on MRI detection of unstable plaques (IMPROVE), can better assess stroke risk and help determine which patients do or do not need surgery. We are investigating whether this method is at least as effective as the standard approach, which mainly considers the degree of narrowing. We expect that this new method will help reduce strokes and lower healthcare costs.

Patients will be followed for several years to compare which method is better for health and costs.

Recruiting

Interested in participating?

Request Info

Key information

About this study

SUMMARY:

Stroke is the 2nd leading global cause of death and disability. Rupture of a vulnerable carotid plaque causes ~20% of ischemic strokes. Symptomatic patients with carotid stenosis may benefit from surgical removal of the plaque or stenting (revascularisation) to prevent recurrent stroke, but this carries risks. Current patient selection for revascularisation is suboptimal, largely based on stenosis degree without considering plaque vulnerability. Improving risk prediction is therefore crucial and has been formally recognized as a key priority in the Dutch Society for Vascular Surgery's Knowledge Agenda (2022): "How can we better identify patients with carotid stenosis who would or would not benefit from revascularisation?" Presence of intraplaque haemorrhage (IPH) on MRI is one of the most powerful imaging biomarkers of plaque vulnerability and a superior predictor of stroke compared to traditional clinical factors, including degree of stenosis. The recently developed "Individualized MRI- Based Stroke Prediction Score Using Plaque Vulnerability for Symptomatic Carotid Artery Disease Patients" (IMPROVE) clinical prediction model integrates both IPH on MRI and clinical risk factors to calculate ipsilateral ischemic stroke risk. This model has demonstrated significantly improved predictive performance over existing scores. A recent decision-analytic study investigated the impact of the use of IMPROVE to select patients with high stroke risk for revascularisation plus OMT (medication and lifestyle advice) and low-risk patients for OMT (optimized medical therapy)-only. This decision-analytic study showed that implementation of the IMPROVE decision rule for revascularisation selection can lead to 35% less ipsilateral strokes and perioperative strokes and deaths and a lifetime cost reduction of €6101 per patient, equating to an annual reduction in societal healthcare costs of €18 million in the Netherlands alone.

Rationale: Patient selection for carotid revascularisation to prevent recurrent strokes could be optimised by providing clinicians and patients the IMPROVE score for shared decision-making. Objective: The primary objective is to investigate the clinical impact and the cost-effectiveness of the individualised MRI-based IMPROVE decision rule compared to care as usual (CAU) in the selection of TIA and non-disabling stroke patients with 30-99% carotid stenosis for revascularisation.

Study design: Multicentre, randomized controlled non-inferiority trial. Study population: Patients with a recent TIA or minor ischemic stroke and ipsilateral 30-99% carotid stenosis according to NASCET criteria.

Intervention: For patients that are randomised to the IMPROVE arm, the IMPROVE risk score will be provided as additional information for clinical decision-making on patient stratification for carotid revascularisation plus OMT versus OMT-only. A revascularization procedure in combination with OMT will be advised for patients at high ipsilateral stroke risk (≥10% within 3 years) according to the IMPROVE score, while OMT- only (medication and lifestyle advice) is advised to patients with lower risk scores.

Comparator: Patients randomised for the control arm (care-as-usual (CAU)) will be selected for revascularisation based on the guidelines for carotid interventions from the European Society for Vascular Surgery. It advises to consider revascularisation for TIA and stroke patients with ≥50% carotid stenosis. Patients with 30-49% stenosis are treated by OMT-only (medication and lifestyle advice). Plaque vulnerability is not taken into account for patient selection in current clinical care in the Netherlands.

Main study parameters/endpoints: Primary: Composite of any stroke or death within 44 days after randomisation or ipsilateral ischemic stroke at any time during subsequent 3-5 years follow up. Secondary: a.o. QALYs, number of revascularization procedures, costs.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Mentally competent
  • 18 years or older
  • Recent (<30 days) stroke (modified Rankin scale ≤3) or TIA
  • Ipsilateral 30-99% atheromatous stenosis at the carotid bifurcation assessed using non-invasive imaging according to NASCET criteria
  • Life expectancy >5 years
  • Patient and stenosis are suitable for carotid revascularisation
  • Patient is agreeable to randomisation and willing to accept either IMPROVE-based or CAU-based selection method for carotid revascularisation

Exclusion criteria

  • Cardiac source of embolism
  • Carotid stenosis caused by non-atherosclerotic disease e.g. dissection, fibromuscular disease or neck radiotherapy.
  • MRI contra-indications
  • Pregnancy

Treatment and study plan

IMPROVE Risk Model

Other

All patients are screened in routine care for stenosis. The stroke risk is assessed using IMPROVE, incorporating plaque vulnerability (intraplaque haemorrhage (IPH) on MRI), stenosis degree, ischemic event type (ocular vs. cerebral), age and sex. The practitioner and patient discuss treatment options in shared decision making based on this risk score. Patients above the risk threshold (≥10% ipsilateral stroke risk within 3 years) receive a recommendation for revascularisation, those below an advice for OMT-only. The 10% threshold resulted in the largest stroke reduction in the decision analytic study. ~53% of the patients need an extra MRI. In ~47% an MRI is unnecessary since, based on the other risk factors, the stroke risk is already high or low and the MRI result does not affect the risk category.

Other names: IMPROVE Rule, IMPROVE Decision Rule, IMPROVE Risk Score, IMPROVE Stroke Risk Model, IMPROVE MRI-Based Model, IMPROVE Risk Stratification, IMPROVE Clinical Decision Tool, IMPROVE Risk Assessment

Primary outcomes

  1. The primary outcome of the study is the composite of any stroke or death within 44 days after randomisation or ipsilateral ischemic stroke at any time during subsequent follow-up.

    Time frame: any strokes/deaths: from randomisation (day 1) until day 44. Ipsilateral ischemic strokes: from randomisation (day 1) through completion of follow-up (36 up to 60 months).

    The perioperative period for the primary endpoint is defined as 44 days after randomisation for both study arms, rather than (the frequently defined) 30 days after carotid revascularisation. This approach avoids bias that would arise if the perioperative window were limited only to patients undergoing revascularisation. By using a fixed 44-day period after randomisation, carotid revascularisation can take place up to two weeks after randomisation without affecting the primary outcome definition, ensuring a fair comparison between treatment arms. The endpoint includes any stroke, including haemorrhagic stroke, as well as death occurring within this period.

Secondary outcomes

  1. Incidence of other cardiovascular ischemic symptoms (any stroke, myocardial infarction, TIA)

    Time frame: From randomisation (Day 1) through completion of follow-up (36 up to 60 months).

  2. Functional outcome (mRS)

    Time frame: At day 44 and 3 years after randomisation.

    The modified Rankin Scale (mRS) is a measure used to assess a patients functional outcome after a stroke. It is an observational scale in which patients are classified into seven categories according to their functional status. A score of "0" corresponds to no symptoms, and a score of "6" corresponds to death.

  3. The iMTA (Institute for Medical Technology Assessment) Productivity Cost Questionnaire (iPCQ)

    Time frame: From baseline follow-up visit through completion of follow-up (36 up to 60 months).

    The goal of the iMTA Productivity Cost Questionnaire (iPCQ) is to measure productivity losses due to health problems for use in economic evaluations and health economic studies.

    Outcomes are reported in (working) days/hours or efficiency loss and there is no fixed total score. Higher values indicate worse productivity loss (e.g. more days absent due to illness or more symptoms during work).

  4. Quality of life (EQ-5D-5L: EuroQol [Quality of Life-5 dimensions-5 levels]) questionnaire

    Time frame: From baseline follow-up visit through completion of follow-up (36 up to 60 months).

    The descriptive system comprises 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems (=0) up to extreme problems (=5). The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state (Dutch value set).

    The EQ VAS (virtual analogue scale) records the patient's self-rated health on a vertical visual analogue scale where the endpoints are labelled 'The best health you can imagine' = 100 and 'The worst health you can imagine' = 0. The VAS can be used as a quantitative measure of health outcome that reflects the patient's own judgement.

  5. The iMTA Medical Consumption Questionnaire (iMCQ)

    Time frame: From baseline follow-up visit through completion of follow-up (36 up to 60 months).

    The iMCQ collects data on medical resource use so that direct healthcare costs can be calculated.

    Assesses healthcare utilization (e.g., visits, hospitalizations, medication use). Outcomes are reported as frequencies/volumes and there is no fixed total score. Higher volumes/frequenties indicate more healthcare use (and therefore higher costs).

  6. Number of hospitalizations

    Time frame: From randomisation (Day 1) through completion of follow-up (36 up to 60 months).

  7. Number of carotid revascularisation procedures

    Time frame: From randomisation (Day 1) through completion of follow-up (36 up to 60 months).

    The number of carotid revascularisations (carotid endarterectomy (CEA) and stenting) will be determined.

  8. Incremental cost-effectiveness ratio

    Time frame: From randomisation (Day 1) through completion of follow-up (36 up to 60 months).

  9. Perioperative complications

    Time frame: From randomisation (Day 1) through completion of follow-up (36 up to 60 months).

Other outcomes

  1. Proportion of patients undergoing carotid revascularisation before application of the decision rule.

    Time frame: From randomisation (Day 1) up to moment of revascularisation.

    Process variables will be measured for the purpose of facilitating further implementation. These process variables are measured only in the intervention group.

  2. Missing MRI or other required input data for application of the decision rule, recorded as the proportion of patients with incomplete data and documented reasons.

    Time frame: From randomisation (Day 1) up to moment of clinical decision making.

    Process variables will be measured for the purpose of facilitating further implementation. These process variables are measured only in the intervention group.

  3. Elective carotid revascularisation in low-risk patients according to the decision rule, assessed as the proportion of patients undergoing elective carotid endarterectomy or carotid artery stenting.

    Time frame: From randomisation (Day 1) up to moment of revascularisation.

    Process variables will be measured for the purpose of facilitating further implementation. These process variables are measured only in the intervention group.

  4. Non-adherence to the risk-based recommendation, assessed as the proportion of patients with treatment decisions deviating from the decision rule.

    Time frame: At moment of clinical decision making (within 14 days after first consult with neurologist).

    Process variables will be measured for the purpose of facilitating further implementation. These process variables are measured only in the intervention group.

  5. Inability to apply the decision rule, assessed as the proportion of patients for whom the decision rule could not be applied, with documented reasons.

    Time frame: At moment of clinical decision making (within 14 days after first consult with neurologist).

    Process variables will be measured for the purpose of facilitating further implementation. These process variables are measured only in the intervention group.

Study contacts

Contact information is provided by the study sponsor or research team.

M. Eline Kooi, Prof. dr.

CONTACT

[email protected]

+31 43 387 4911

Robin M.M. Pleumeekers, MSc.

CONTACT

[email protected]

+31 43 387 7622

Sponsors and collaborators

Lead sponsor

Maastricht University Medical Center

Other

Collaborators

  • Academisch Ziekenhuis Maastricht
  • Albert Schweitzer Hospital
  • Amsterdam UMC
  • Erasmus Medical Center
  • Haaglanden Medical Centre
  • Isala
  • Radboud University Medical Center
  • Rijnstate Hospital
  • UMC Utrecht
  • Zuyderland Medical Centre

Registry information

Official study title

Clinical Impact of the Use of IMPROVE for Selection of Patients for Carotid Revascularisation: a Randomized Controlled Multicentre Non-inferiority Trial in Symptomatic Patients With 30-99% Carotid Stenosis

Acronym: IMPROVE

Important dates

Study start
2026
Primary completion
2028
Study completion
2031
First posted
Apr 29, 2026
Registry last updated
May 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.