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Clinical controlled trial study on the recanalization and conservative treatment of occlusion /sub total occlusion of middle cerebral artery M1 segment

Clinical controlled trial study on the recanalization and conservative treatment of occlusion /sub total occlusion of middle cerebral artery M1 segment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCC-15006807
Enrollment
Unknown
Registered
2015-07-24
Start date
2015-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

the M1 segment of the MCA occlusion / subtotal occlusion

Interventions

Interventional procedure :Percutaneous middle cerebral artery angioplasty
Conservative treatment:Medication

Sponsors

The first affilliated hospita of Zhengzhou university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-80 years; 2. Clinical symptoms; 3. CTA, MRA or DSA confirmed with the M1 segment of the MCA occlusion / subtotal occlusion; 4. PWI showed occlusion of the M1 segment of the MCA / subtotal occlusion of the contralateral hypoperfusion; 5. Glasgow Coma Scale (GCS) scores were more than or equal to 12 points; 6. Informed consent must be signed.

Exclusion criteria

Exclusion criteria: 1. Coagulation dysfunction; 2. Suffering from malignant tumor (the expected survival time less than 1 years); 3. Contrast agent allergy; 4. With cerebral hemorrhage history (ipsilateral middle cerebral artery regional); 5. Intracranial operation history or severe head injury history in the last 3 months; 6. Hmorrhage in digestive tract, urinary tract or other organs in the last 3 weeks; 7. Surgery operation historyrecent in last 2 weeks; 8. Blood pressure can not be stable controled; 9. Antiplatelet drug intolerance; 10. Bilateral middle cerebral artery occlusion; 11. The blood vessel is invalid (the occlusion of middle cerebral artery lead a large area of cerebral infarction).

Design outcomes

Primary

MeasureTime frame
PWI;

Secondary

MeasureTime frame
NHISS score;

Countries

China

Contacts

Public ContactHan Xinwei
hanxinwei2006@163.com+86 13803842129

Outcome results

None listed

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