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Selective intracerebral arterial hypothermia combined with endovascular treatment for acute ischemic stroke

Selective intracerebral arterial hypothermia combined with endovascular treatment for acute ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087155
Enrollment
Unknown
Registered
2024-07-22
Start date
2025-02-20
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

ischemic stroke

Interventions

combining treatment group:After randomization, mechanical thrombectomy are performed to open blood flow, balloon plasty, stenting and other remedial treatments are still included in the study. After
Endovascular interventional therapy alone group:Blood flow opening (mechanical thrombectomy, thrombus extraction, balloon forming, stent placement, etc.)is performed routinely, without cold saline per

Sponsors

Hubei No.3 People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age over 18 years; 2) The time from onset to randomization is within 24h; 3) Acute ischemic stroke was clinically diagnosed; 4) mRS 0-1 score before the stroke; 5) NIHSS score >=6 before randomization; 6) CT ASPECTS score >=3 before randomization; 7)CTA/MRA/DSA confirmed acute occlusion in the following parts: intracranial segment of internal carotid artery, M1 segment of middle cerebral artery, and main segment of M2 segment of middle cerebral artery; 8) Consent to endovascular therapy; 9) Written informed consent signed by the patient or his legal representative.

Exclusion criteria

Exclusion criteria: 1)CT or MRI suggest intracranial hemorrhage. 2) Pregnant or lactating women; 3) Severe allergy to contrast media; 4) Systolic blood pressure > 220mm Hg or diastolic blood pressure > 110mm Hg, and cannot be controlled by antihypertensive drugs; 5) Genetics or acquired bleeding constitution, lack of anticoagulation factors; Or have taken oral anticoagulants and INR> 3.0; 6) Blood glucose 22.2mmol/L(400mg/dl); 7) Severe renal insufficiency (glomerular filtration rate 220umol/L(2.5mg/dl)); 8) History of bleeding (gastrointestinal and urinary tract bleeding) in the past 1 month; 9) Severe infection; 10) Intracranial aneurysm, arteriovenous malformation; 11) Brain tumors with space occupying effect on imaging; 12) Life expectancy < Six months; 13) Participating in other clinical trials; 14) The follow-up is not expected to be completed.

Design outcomes

Primary

MeasureTime frame
Score of 0–2 on the modified Rankin Scale ;

Secondary

MeasureTime frame
mRS score at 90 days;

Countries

China

Contacts

Public ContactYue Wan

Hubei No.3 People's Hospital of Jianghan University

Wanyue790623@163.com+86 158 2715 2880

Outcome results

None listed

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