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A multicenter clinical study on the treatment of moyamoya disease with a new type of side-to-side anastomotic

A multicenter clinical study on the treatment of moyamoya disease with a new type of side-to-side anastomotic

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059220
Enrollment
Unknown
Registered
2022-04-27
Start date
2023-01-18
Completion date
Unknown
Last updated
2024-02-19

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

Conditions

Moyamoya Disease

Interventions

side to side anastomosis group:side to side anastomosis "flow self-regulated bypass surgery"
end to side anastomosis group:Conventional end to side anastomosis "flow control bypass surgery"

Sponsors

Zhongnan hospital of Wuhan university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: A. patient aged between 6 to 75; B. Diagnostic criteria of moyamoya disease. Diagnosis by digital subtraction angiography (DSA) is based on the following criteria: (1) arterial stenosis or occlusion at the end of the ICA and/or the initial segment of the MCA and/or ACA; (2)Moyamoya-like vascular network is present; (3) Other diseases associated with moyamoya syndrome (MMS) are excluded, such as intracranial atherosclerosis, systemic vasculitis, Down syndrome, acute stroke, hyperthyroidism, meningitis , neurofibromatosis, previous skull base radiation therapy, leptospirosis infection, or autoimmune disease; C. Meet the surgical indications of moyamoya disease. The surgical indications should comply with the 2012 Japanese guidelines for the diagnosis and treatment of moyamoya disease: (1) there have been disease-related symptoms of cerebral ischemia, including TIA, reversible ischemic neurological deficit, cerebral infarction, cognitive decline, limb involuntary movement, headache and seizures; (2) Evidence suggests that there is a decline in cerebral blood flow reserve, including local cerebral blood flow and cerebral blood flow reserve; (3) Presence of disease-related intracerebral hemorrhage and exclusion of other causes; (4) Other surgical contraindications were excluded;

Exclusion criteria

Exclusion criteria: Patients who were unable to follow up or refused to follow up due to other diseases or accidental deaths after surgery

Design outcomes

Primary

MeasureTime frame
Bypass success rate;Changes of cerebral blood flow during and after operation;Perioperative complications: hyperperfusion and blood flow hedging;Revascularization effect after operation;Influence on cognitive function of patients;Improvement of the patient's clinical symptoms;

Secondary

MeasureTime frame
Incidence of major clinical events 1 year after primary surgery;The bypass success rate of 1 year after the first operation;

Countries

China

Contacts

Public ContactZhang Jianjian

Zhongnan hospital of Wuhan university

zj57470@126.com+86 18971352943

Outcome results

None listed

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