Evaluate the Accuracy of Raman IVD Analyzer in the Diagnosis of Gliomas During Surgery
NCT ID: NCT05901844
Last Updated: 2023-06-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
256 participants
INTERVENTIONAL
2023-06-30
2024-10-31
Brief Summary
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Detailed Description
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During surgery, core or marginal tissue samples were taken from subjects. The test samples size:0.2cm\<length diameter ≤ 2cm. The sample testing result is based on the Raman test points. Then take the same tissue sample for paraffin pathological diagnosis.
Statistical description of all data, including baseline data, all efficacy indicators, and all safety data. The measurement data give the mean, standard deviation, minimum, maximum, median,25 quantile and 75 quantile; Provide frequency and composition ratio for counting data. The baseline data was analyzed using the Full Analysis Set (FAS); The effectiveness analysis adopts FAS and PPS; The security analysis uses the Security Dataset (SS).
Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Perform two different tests on the same sample
The same sample is diagnosed using a Raman analyzer firstly and then diagnosed by paraffin pathology.
Paraffin pathological diagnosis
Perform two diagnostic methods on the same sample
Interventions
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Paraffin pathological diagnosis
Perform two diagnostic methods on the same sample
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patients who plan to undergo brain lesion tissue resection surgery or have preoperative clinical diagnosis of gliomas and plan to undergo biopsy;
* Patients with clinical diagnosis of initial solitary gliomas, or initial solitary intracranial masses or initial non occupying lesions that do not exclude gliomas (such as intracranial metastatic lesions, intracranial infectious lesions, intracranial demyelinating lesions, central nervous system lymphoma, etc.), who have not received radiotherapy or chemotherapy in the past based on their medical history;
* The patient or their guardian can understand the research purpose, demonstrate sufficient compliance with the trial protocol, and sign an informed consent form;
* It is possible to obtain tissue samples with a length diameter greater than 0.2cm. Patients diagnosed with initial solitary glioma should take core or marginal tissue, while patients diagnosed with initial single intracranial mass or initial non mass lesions but maybe with gliomas should be taken core tissue.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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West China Hospital
OTHER
The First Affiliated Hospital of Zhengzhou University
OTHER
Capital Medical University
OTHER
Jiangsu Raman Medical Equipment Co., Ltd.
INDUSTRY
Beijing Tiantan Hospital
OTHER
Responsible Party
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Principal Investigators
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Tao Jiang, MD and PhD
Role: PRINCIPAL_INVESTIGATOR
Beijing Tiantan Hospital
Qing Mao
Role: PRINCIPAL_INVESTIGATOR
West China Hospital
Dongming Yan
Role: PRINCIPAL_INVESTIGATOR
The First Affiliated Hospital of Zhengzhou University
Shouwei Li
Role: PRINCIPAL_INVESTIGATOR
Capital Medical University
Central Contacts
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Other Identifiers
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LRR202301
Identifier Type: -
Identifier Source: org_study_id
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