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Application of Multimodal Functional Neuro-navigation Combined with Intraoperative Fluorescein Sodium and Intraoperative Ultrasound in Surgery for Intracranial Malignant Tumors

Application of Multimodal Functional Neuro-navigation Combined with Intraoperative Fluorescein Sodium and Intraoperative Ultrasound in Surgery for Intracranial Malignant Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110401
Enrollment
Unknown
Registered
2025-10-13
Start date
2025-10-13
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Intracranial malignant tumor

Interventions

Trial Group:Functional neuro-navigation combined with intraoperative fluorescein sodium and intraoperative ultrasound
Control group:Functional neuro-navigation

Sponsors

Inner Mongolia Autonomous Region People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. None of them had received radiotherapy or chemotherapy before the operation. 2. Before the operation, they had no unconsciousness and were able to cooperate with the examination. 3.Through imaging examinations, the tumor was located above the tentorium cerebelli. 4.The first surgery was performed and the pathological diagnosis was intracranial malignant tumor (grade ? - ?).

Exclusion criteria

Exclusion criteria: 1. Those with severe heart, liver, kidney or other major diseases. 2. Those who cannot tolerate enhanced examinations. 3.Those with a history of cerebral hemorrhage, extensive cerebral infarction or other intracranial occupying lesions in the past. 4.Those who are allergic to sodium fluorescein. 5.Pregnant women and other patients who cannot undergo surgical treatment.

Design outcomes

Primary

MeasureTime frame
Tumor resection rate;Extent of tumor resection;Tumor volume;Functional improvement (including comparison of changes in functional impairment based on KPS score between preoperative and 3-month postoperative periods, and comparison of changes in muscle strength from preoperative to discharge between the two groups).;

Secondary

MeasureTime frame
Progression free survival (PFS);New-onset neurological deficit;Postoperative complications (including observation for epilepsy, intracranial infection, and pulmonary infection).;Surgery time;

Countries

China

Contacts

Public ContactWang Zhong

Inner Mongolia Autonomous Region People's Hospital

wz1971@163.com+86 180 4719 2566

Outcome results

None listed

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