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Clinical study on the safety and efficacy of hyperspectral imaging to determine glioma boundary and rapid pathological diagnosis

Clinical study on the safety and efficacy of hyperspectral imaging to determine glioma boundary and rapid pathological diagnosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072035
Enrollment
Unknown
Registered
2023-06-01
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Glioma

Interventions

Gold Standard:HE stained specimen sections
Index test:Hyperspectral imaging, HSI

Sponsors

Tangdu Hospital, Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-70 years old, gender unlimited; (2) glioma patients to be treated by surgery. (3) Subjects voluntarily participate in this study and sign informed consent, and can understand and comply with the requirements of the study.

Exclusion criteria

Exclusion criteria: (1) Unable to perform MRI scanning and other imaging examinations; (2) Heart failure of grade III and IV (NYHA grade), unstable angina pectoris, acute myocardial infarction, persistent and clinically significant arrhythmia occurred within 6 months before enrollment; (3) Major surgery (excluding glioma surgery) was performed within 4 weeks before enrollment; Those who had bone marrow biopsy, open biopsy and intracranial biopsy within 7 days before screening; And other patients with high-risk factors for bleeding (4) Pregnant or lactating women, or those who plan to become pregnant during the study period; (5) Those who participated in other clinical trials within 30 days before enrollment; (6) The investigator judged that it was not suitable to participate in this clinical trial

Design outcomes

Primary

MeasureTime frame
Boundary accuracy;

Secondary

MeasureTime frame
Survival time;Progression-Free Survival;Karnofsky Performance Status;Quality of Life score (EORTC QLQ-C30 and EORTC QLQ-BN20);

Countries

China

Contacts

Public ContactWang Yuan

Tangdu Hospital, Airforce Medical University

drwangyuan@88.com+86 153 5362 1583

Outcome results

None listed

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