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A clinical application study of a stent placement assessment

A clinical application study of a stent placement assessment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055890
Enrollment
Unknown
Registered
2022-01-22
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Acute ischemic stroke

Interventions

Study group:Operated according to the ECASES system
Control group :Operated according to operator experience

Sponsors

Tianjin Huanhu Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-80 years old, regardless of gender. 2.Preoperative NIHSS score = 6. 3.An ASPECTS score of =6 based on MRI-DWI sequences. 4.The time from onset to the expected start of endovascular treatment was =24 hours, with patients between 6 and 16 hours meeting the inclusion criteria for the DAWN study and the DEFUSE 3 study, and patients between 16 and 24 hours meeting the inclusion criteria for the DAWN study. 5.Pre-stroke MRS score of 0-1. 6.Life expectancy = 2 years. 7.Patients and their families agreed to the endovascular treatment and this study protocol and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with combined intracranial hemorrhage confirmed by CT or MRI are excluded. 2.Patients with a combination of severe renal insufficiency (creatinine > 264 µmol/L), respiratory and circulatory instability, severe coagulation dysfunction (INR > 3.0 or PTT > 3 times normal) and other contraindications to interventional procedures are excluded. 3.Patients with pre-existing neurological or psychiatric disorders that could confound the evaluation of the results were excluded. 4.Uncontrollable hypertension Systolic blood pressure >185 mmHg Diastolic blood pressure >110 mmHg. 5.Platelet count 22.20 mmol/L. 7.Those who cannot undergo cranial MRI. 8.Patients deemed unsuitable for study participation by other investigators.

Design outcomes

Primary

MeasureTime frame
NIHSS score;mRS score;

Secondary

MeasureTime frame
Changes in neurological function;Intracranial hemorrhage;Cerebral edema;mTICI grading;New cerebral infarction;Reocclusion of the responsible vessel;

Countries

China

Contacts

Public ContactHecheng Ren

Tianjin Huanhu Hospital

doctorrenhecheng@126.com13820759606

Outcome results

None listed

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