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Completed

NCT Number: NCT04904419

Multi-center Research Project for Glioma Molecular Pathology Intraoperative Rapid Detection

We explores the accuracy and sensitivity of rapid intraoperative detection of IDH, TERT, BRAF indicators through a prospective clinical multi-center study. This part includes a total of 300 fresh tissue samples, paired blood samples, relevant clinical information and follow-up information from 300 patients with different grades of adult glioma. By comparing with the postoperative sequencing results, the specificity and sensitivity of intraoperative IDH and TERT rapid detection results are clear.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The First Affiliated Hospital of Fujian Medical University, Fuzhou, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Glioma patients with Informed Consent Form 2. Glioma patients with intact clinical information

Exclusion criteria

  • 1. Glioma patients without Informed Consent Form 2. Glioma patients without intact clinical information

Treatment and study plan

Intraoperative Rapid Detection mutation of IDH, TERT and BRAF v600e

Diagnostic Test

Intraoperative Rapid Detection mutation of IDH, TERT and BRAF v600e

Primary outcomes

  1. Intraoperative Rapid Detection mutation of IDH, TERT and BRAF v600e

    Time frame: Intraoperative Rapid Detection mutation of IDH, TERT and BRAF v600e

Sponsors and collaborators

Lead sponsor

Jinsong Wu

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
May 27, 2021
Registry last updated
Apr 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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