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Screening and identification of the therapeutic efficacy and molecular mechanism of oncolytic viruses on glioma based on organoid culture technology: A prospective real-world study

Screening and identification of the therapeutic efficacy and molecular mechanism of oncolytic viruses on glioma based on organoid culture technology: A prospective real-world study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104659
Enrollment
Unknown
Registered
2025-06-20
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Glioma

Interventions

Oncolytic virus detection group of organoids:NA

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 70 years old; 2. Karnofsky Performance Status (KPS) score >= 60; 3. The diagnosis by histopathology was primary/recurrent glioblastoma. 4. Patients with measurable or evaluable lesions confirmed by MRI, with an expected survival of at least 12 weeks, and who consent to surgical resection of the lesion. 5. Have sufficient bone marrow function to receive subsequent adjuvant therapy (white blood cell count >= 4000/µL, neutrophil count >= 1500/µL, platelet count >= 100,000/µL, hemoglobin >= 8.0g/dL), renal function (serum creatinine <= 150µmol/L, 24-hour urine protein <= 3.4g) and liver function (total bilirubin <= 34µmol/L, aspartate and alanine aminotransferase <= 120U/L). 6. The patient is capable of understanding and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Extracranial metastatic disease; 2. Has received or is currently undergoing treatment with carmustine wafer implants (Gliadel); 3. Severe cardiopulmonary insufficiency; 4. status epilepticus; 5. Pregnant or lactating women; 6. gastrointestinal bleeding; 7. Blood pressure (>140/90mmHg) after uncontrolled medication use; 8. There are frequent vomiting, difficulty in swallowing or other conditions that affect oral administration of drugs. 9. HIV positive and antiretroviral therapy; 10. Patients who are currently participating in other clinical trials or have previously participated and have not yet completed the trials. 11. Other conditions that the researchers consider unsuitable for participation in this trial.

Design outcomes

Primary

MeasureTime frame
Overall survival;objective response rate;

Countries

China

Contacts

Public ContactGuanglong Huang

Southern Medical University Southern Hospital

hgl1020@163.com+86 20 61641806

Outcome results

None listed

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