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2024-516642-19-01CompletedPhase 4

HOPE study

A randomized trial on Hemodynamic Optimization of cerebral Perfusion after Endovascular therapy in patients with acute ischemic stroke (HOPE study)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 7 Jul 2025

Next steps

Brief summary (registry, in English)

Compare the clinical benefit of standard blood pressure management after mechanical thrombectomy versus a specific protocol aimed at hemodynamic optimization, where blood pressure targets are applied based on the degree of recanalization achieved during the procedure. Compare the clinical benefit of standard blood pressure management after mechanical thrombectomy versus a specific protocol aimed at hemodynamic optimization, where blood pressure targets are applied based on the degree of recanalization achieved during the procedure.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
814 (actual)
First submitted
5 Nov 2024
Start date
16 Jun 2021
Lead sponsor
Fundacio Institut De Recerca De L'Hospital De La Santa Creu I Sant Pau
Diseases
Stroke
EU CT number
2024-516642-19-01
EudraCT number
2021-000022-10

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 814
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of MAO inhibitors

Other illness

  • History of intracerebral hemorrhage
  • Patient with congestive heart failure or unstable or recent coronary artery disease (<3 months)
  • Any visible hemorrhage on the initial CT scan
  • History of ventricular arrhythmias

Other

  • ASPECTS score < 6
  • Inclusion in other clinical trials.
  • Occlusion in the vertebral, basilar, A2, P2, and M3-4 arteries.
  • Pregnant or lactating patient
  • Dissection of the aorta, cervical, or cerebral arteries, or unruptured aortic/cerebral aneurysm or known arteriovenous malformation

Who the study is looking for

  • Patients with acute ischemic stroke and large intracranial vessel occlusion within 24 hours of symptom onset who have undergone mechanical thrombectomy.
  • Successful recanalization, defined as a TICI score of 2b, 2c, or 3.
  • Prior score on the modified Rankin Scale (mRS) of 0, 1, or 2.
  • The patient or their legal representative provides informed consent in writing or verbally.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (15)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hospital General Universitario Dr. BalmisAlicanteSpainCompleted
Hospital Universitario de CrucesBarakaldoSpainCompleted
Hospital de la Santa Creu i Sant PauBarcelonaSpainCompleted
Hospital del MarBarcelonaSpainCompleted
Hospital Universitari de Girona Doctor Josep TruetaGironaSpainCompleted
University Clinical Hospital Virgen De La ArrixacaMurciaSpainCompleted
Hospital Universitario Central De AsturiasOviedoSpainCompleted
Hospital Universitario De SalamancaSalamancaSpainCompleted
Complexo Hospitalario Universitario De SantiagoSantiago de CompostelaSpainCompleted
University Hospital Virgen Del Rocio S.L.SevillaSpainCompleted
Hospital Universitari Joan XXIII de TarragonaTarragonaSpainCompleted
Hospital Universitario Y Politecnico La FeValenciaSpainCompleted
Hospital Clinico Universitario de ValenciaValenciaSpainCompleted
Hospital Universitario Miguel ServetZaragozaSpainCompleted
Complexo Hospitalario Universitario A Coruña (La Coruña, Spain)-SpainCompleted

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.