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Ultra-early STatin in patients with Aneurysmal subaRachnoid hemorrhage (Ue-STAR): a randomized controlled trial

Ultra-early STatin in patients with Aneurysmal subaRachnoid hemorrhage (Ue-STAR): a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088277
Enrollment
Unknown
Registered
2024-08-14
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Aneurysmal Subarachnoid Hemorrhage

Interventions

Statin group:On the basis of routine treatment for aneurysmal subarachnoid hemorrhage, atorvastatin was administered at an ultra early stage at a dose of 40mg/d for 14 consecutive days
Conventional treatment group:Conventional treatment for aneurysmal subarachnoid hemorrhage typically includes measures such as blood pressure control, hemostasis, reduction of intracranial pressure, p

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Male or female; aged 18 years or over; 2.Signs and symptoms presumed aneurysmal subarachnoid hemorrhage, confirmed by radiological evidence; 3.Treatment within 6 hours after symptom onset.

Exclusion criteria

Exclusion criteria: 1.Treatment with statin prior SAH; 2.Non-aSAH (e.g. traumatic subarachnoid hemorrhage, arteriovenous malformation); 3.Treatment > 6 hours after symptom onset; 4.Allergy to statin medications or presence of severe adverse reactions such as abnormal liver function or rhabdomyolysis; 5.Evidence of irreversible brain damage or expected death within 7 days; 6.Known severe liver or kidney disease; 7.Non-compliance with follow-up; 8.Pregnant or breastfeeding; 9.History of severe cranial or psychiatric illness; 10.Concomitant serious systemic disease; 11.Patients with malignant tumors; 12.Currently participating in another clinical trial; 13.Considered unsuitable for the clinical trial by clinical physicians or researchers.

Design outcomes

Primary

MeasureTime frame
Utility-Weighted Modified Rankin Scale;

Secondary

MeasureTime frame
Modified Rankin Scale (mRS) Score;GOSE, Glasgow Outcome Scale;EQ-5D-5L;

Countries

China

Contacts

Public ContactRongcai Jiang

Tianjin Medical University General Hospital

jiang116216@163.com+86 136 7211 6556

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026