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NCT Number: NCT04651010

Predictive Multimodal MRI Factors in Subacute Cerebral Artery Occlusiontreated by Thrombectomy (PIMISUTT)

Our study aims to measure metabolic and functional parameters of the infarcted territory by multimodal cerebral MRI in patients diagnosed with unilateral proximal occlusion of the middle cerebral artery and treated by thrombectomy in order to correlate those parameters to clinical outcome (evaluated by modified Rankin score) at 3 months.

We aim to find early radiologic predictive factors for favorable clinical outcome in this population of patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Poitiers

Poitiers, France

Location status: Recruiting

Location contact

Guillaume HERPE, Dr

CONTACT

About this study

The treatment of acute ischemic stroke in the setting of intracranial large artery occlusion and especially middle cerebral artery occlusion (MCAO) with intravenous tissue plasminogen activator (IV-tPA) is associated with low rates of recanalization and high rates of neurological morbidity and functional dependence.

In the last few years, endovascular intervention (mechanical thrombectomy) has proven its safety and its efficacy on clinical outcome in patients diagnosed with MCAO and is now commonly recommended.

However, in this population of patients treated by thrombectomy, very few predictive factors, except for the post-procedural recanalization score (TICI), do exist to foresee the variability of clinical outcome.

Tissue viability of the infarcted territory can be approached by the measure of metabolic and morphological parameters (Na+, H+, phosphore, diffusion imaging) which can be non-invasively done by multimodal MRI, as suggest by recently published studies.

Our study plans to measure these parameters between 12 and 24 hours after acute ischemic stroke in patients with MCAO treated by thrombectomy in order to correlate those parameters to clinical outcome at 3 months (modifier Rankin Score).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients aged ≥ 18 years old
  • Hospitalized at the Poitiers University Hospital
  • Acute middle cerebral artery occlusion diagnosed by CT-scan or MRI
  • NIHSS score ≥ 6 at admission
  • To be treated by thrombectomy with or without fibrinolysis
  • Written information delivered to the patient or his relatives concerning the study and its benefit and risk

Exclusion criteria

  • Patients or relatives whom a loyal information about the study cannot be given
  • Patient with cognitive impairments before MRI.
  • Patients who cannot undergo MRI because of contraindications
  • Patients too deteriorated to tolerate one hour long exam

Treatment and study plan

Multimodal MRI

Other

Multimodal MRI will be realized between 12 and 24 hours after thrombectomy

Primary outcomes

  1. Correlation between modified Rankin score at 3 months and multimodal MRI data

    Time frame: Month 3

Secondary outcomes

  1. Discharge National Institute of Health Stroke Score (NIHSS)

    Time frame: Month 3

  2. National Institute of Health Stroke (NIHSS) score at 3 months

    Time frame: Month 3

  3. Change in NIHSS score at 3 months compared to post-thrombectomy

    Time frame: Month 3

Study contacts

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

Céline DELETAGE

CONTACT

[email protected]

05 49 44 38 54 ext. +33

Guillaume HERPE, Dr

CONTACT

[email protected]

05 49 44 33 89

Sponsors and collaborators

Lead sponsor

Poitiers University Hospital

Other

Registry information

Official study title

Predictive Multimodal MRI Factors in Subacute Cerebral Artery Occlusiontreated by Thrombectomy (PIMISUTT

Acronym: PIMISUTT

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Dec 3, 2020
Registry last updated
May 26, 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.

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