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Clinical trial of whole brain radiotherapy combined with stereotactic radiotherapy for metastatic brain carcinomas

Clinical trial of whole brain radiotherapy combined with stereotactic radiotherapy for metastatic brain carcinomas

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084295
Enrollment
Unknown
Registered
2024-05-14
Start date
2024-05-20
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Metastatic brain carcinomas

Interventions

Sponsors

The First Affiliated Hospital of Chengdu Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age =18 years old, gender unlimited; 2) Histologically confirmed solid malignant tumor at the primary site or metastatic site; 3) Imaging confirmed 5mm extra-marginal brain metastases around the hippocampus (1-3 lesions) (the maximum diameter of a single lesion is 5cm, and the maximum diameter of multiple lesions is not more than 3cm); 4) ECOG score of 0-2, life expectancy of at least 6 months; 5) Not pregnant or breastfeeding; 6) The subject must understand and sign the informed consent 7) Have reading comprehension ability and can complete the questionnaire with medical assistance; 8) Those who voluntarily participate in the study and sign the informed consent letter in person

Exclusion criteria

Exclusion criteria: 1) Previously received craniocerebral radiation therapy; 2) Diffuse meningeal metastasis; 3) Have a mental illness that the investigator believes will interfere with completion of treatment or follow-up; 4) Unable to perform enhanced MRI; 5) Patients with severe underlying diseases who cannot tolerate radiotherapy; 6) Tumor PTV volume > 60cc; 7) The patient was diagnosed with primary brain tumor and primary germ cell tumor; 8) Female patients who are pregnant or breastfeeding; 9) Other cases deemed unsuitable for inclusion by the investigators.

Design outcomes

Primary

MeasureTime frame
Time of intracranial lesion progression;

Secondary

MeasureTime frame
Changes in cognitive function and quality of life;Adverse effects;

Countries

China

Contacts

Public ContactTao Ren

The First Affiliated Hospital of Chengdu Medical College

rentao509@cmc.edu.cn+86 189 8055 6418

Outcome results

None listed

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