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Clinical Trials in China / NCT06201351
Starting soon Observational

Study of Adaptive Radiotherapy for High-grade Glioma Based on Interfraction MRI

NCT06201351 · tracked via the Priya Life Science China tracker
Sponsor
West China Hospital
Phase
Observational
Started
2024-01-01
Last updated
2024-01-11

Condition(s) studied

High-grade Glioma

Investigational drug(s) / intervention(s)

adaptive radiotherapy

adaptive radiotherapy: MRI was performed and adaptive radiotherapy was administered at farction10 and fraction 20 during radiotherapy.

Study summary

The changes of target and organs at risk in patients with high-grade glioma during concurrent chemoradiotherapy were evaluated by MRI image between radiotherapy fractions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥18 years old; 2. High-grade glioma was confirmed by pathology after surgery; 3. ECOG score 0-2 points; 4. Receiving the standard STUPP regimen (i.e. 6 weeks of temozolomide concurrent chemoradiotherapy +6 cycles of temozolomide adjuvant chemotherapy); 5. Baseline data available. Exclusion Criteria: 1. The pathological diagnosis is not clear; 2. No synchronous chemotherapy/adjuvant chemotherapy \< 6 cycles; 3. There are other malignant tumors; 4. Previously radiotherapy to the head; 5. Interruption of radiotherapy for more than 5 days; 6. Failure to collect baseline data.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
West China Hospital Chengdu Sichuan

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06201351 on ClinicalTrials.gov ↗ ← All trials in China