Sonography-guided Resection of Brain Mass Lesions

Study acronym: SOMALI
StatusRecruiting
PhaseNot applicable
Started

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Trial flagged as At Risk
Primary endpoint added 1 → 2 primary endpoints
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Record History

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  1. Primary endpoint(s) modified
    • Eligibility criteria expanded, about 37 words
    • Secondary endpoints: 12 to 10
    • Study description expanded, about 5 words
  2. 2 versions Re-verified since Apr 5, 2024, no change to tracked fieldsv4-v5
  3. Secondary endpoints: 11 to 12v3
  4. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    v2
  5. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The study aims to perform a comparative analysis of preoperative CT/MRI and intraoperative ultrasound findings in patients with hemispheric brain tumors (meningiomas, gliomas, metastases), and to develop an intraoperative ultrasound scanning algorithm for the differential diagnosis of residual tumor tissue and sonographic artifacts within the resection cavity.
Trial Details
NCT Number NCT05484245
Lead Sponsor Sklifosovsky Institute of Emergency Care
Conditions
(from sponsor)		 Tumor, Brain, Meningioma of Brain, Glioma, Metastasis Brain
Related terms Brain Neoplasms, Glioma, Meningioma
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov