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Clinical study on the protective effect of preoperative lumbar drainage on the temporal lobe in petroclival meningioma resection by anterior transpetrous approach

Clinical study on the protective effect of preoperative lumbar drainage on the temporal lobe in petroclival meningioma resection by anterior transpetrous approach - None

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090537
Enrollment
Unknown
Registered
2024-10-08
Start date
2025-02-15
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

Petroclival meningioma

Interventions

experimental group:preoperative lumbar drainage
control group:no preoperative lumbar drainage

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) The ages between of 18 and 75 (including critical values), regardless of gender (2) Meningioma diagnosed firstly through imaging (preoperative enhanced MRI), pathologically confirmed (WHO Central Nervous System Tumor Classification, 5th edition 2021), with surgical indications, not involving the temporal lobe on the surgical side, suitable for anterior petrosal approach (evaluated by the operator based on imaging data) (3) with normal language and no accompanying epilepsy in preoperation (4) KPS score = 70 points (5) Expected survival time = 6 months; (6) Having normal organs and hematopoietic function, normal laboratory tests, and no serious surgical contraindications such as heart, lung, liver, kidney dysfunction, and immune deficiency (7) Voluntarily participate in clinical research and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Excluding intracranial synchronous radiotherapy and chemotherapy (TMZ dosage = 75mg/m2 in synchronous radiotherapy and chemotherapy, radiotherapy dosage is limited to the range of 50-60Gy) (2) Patients receiving treatment with other anti-tumor drugs (including chemotherapy, targeted drugs, immunotherapy, traditional Chinese medicine anti-tumor therapy, electric field therapy, etc.) (3) Individuals who suffer from severe heart disease within the 6 months prior to enrollment, such as unstable angina, myocardial infarction, heart failure (New York Heart Association heart function classification>Grade II), or stroke (excluding lacunar infarction), and unable to tolerate surgery (4) Merge other intracranial tumors such as NF2, multiple meningiomas, brain metastases, or other diseases that damage brain, such as cerebral hemorrhage, cerebral infarction, intracranial infection, etc (5) Previously underwent craniotomy surgery;

Design outcomes

Primary

MeasureTime frame
Temporal lobe injury;

Countries

China

Contacts

Public ContactXin-ru Xiao

Xuanwu Hospital, Capital Medical University

Xiaoxinru_xwyy@126.com+86 133 8127 9170

Outcome results

None listed

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