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SAVIOR (Subarachnoid hemorrhage: clAzosentan vs. fasudIl for VasOspasm pRevention)

The comparison of efficacy and safety between fasudil and clazosentan for the prevention of vasospasm after aneurysmal subarachnoid hemorrhage

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1041240128
Enrollment
714
Registered
2024-11-22
Start date
2025-03-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aneurysmal subarachnoid hemorrhage Subarachnoid hemorrhage, vasospasm

Interventions

For patients who have undergone surgery for ruptured aneurysms, randomized allocation of Fasudil, a conventional drug, or Clazosentan, a novel drug,to prevent cerebral vasospasm after aneurysmal subar
Open-label, randomized, parallel-group comparison

Sponsors

Ryuta Saito
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with subarachnoid hemorrhage due to ruptured cerebral aneurysm 2.Patients who have undergone radical surgery for ruptured cerebral aneurysm within 48 hours of onset 3.World Federation of Neurosurgical Surgeons (WFNS) classification I-V 4.18 years of age or older 5.Modified Rankin Scale (mRS) 0-2 before onset 6.Patients with written consent from the patient or a surrogate (Patients who have difficulty giving consent due to poor level of consciousness should have the purpose of the study explained to the same person who consented to the surgery and consent obtained).

Exclusion criteria

Exclusion criteria: 1.Patients with subarachnoid hemorrhage due to vascular malformations such as cerebral arteriovenous malformation, dural arteriovenous fistula, moyamoya disease, and trauma 2.Patients who have undergone radical surgery for ruptured aneurysms more than 48 hours after onset 3.Patients with a history of hypersensitivity to any component of the drug 4.Pregnant women or patients who may be pregnant 5.Patients with persistent intracranial bleeding 6.Patients in whom adequate intraoperative hemostatic treatment of a bleeding aneurysm could not be performed 7.Patients with severe hepatic dysfunction (Child-Pugh Class C) 8.Patients with severe hypotension (systolic blood pressure less than 80 mmHg) 9.Patients deemed inappropriate by the physician in charge

Design outcomes

Primary

MeasureTime frame
modified Rankin Scale (mRS) at 90 days after onset

Secondary

MeasureTime frame
1.mRS at discharge from acute care unit 2.cerebral vasospasm and cerebral infarction related to cerebral vasospasm 3.salvage therapy for symptomatic cerebral vasospasm (fasudil infusion, balloon catheter angioplasty) 4.all cerebral infarctions (excluding those due to surgical invasion) 5.death (all related to the underlying disease) 6.incidence of hyponatremia and hypoalbuminemia 7.complication rates (symptomatic pleural and pulmonary edema, intracranial hemorrhage, cerebral edema, hypotension) 8.Comparison of primary and secondary endpoints 1-7 between allocation groups in the following populations - Severity of disease according to the WFNS classification - Age (75 years and older/under 75 years old) - Risk of cerebral vasospasm by Fisher classification

Contacts

Public ContactMuraoka Shinsuke

Nagoya University Graduate School of Medicine

muraoka.shinsuke.y2@f.mail.nagoya-u.ac.jp+81-52-744-2353

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026