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Prospective clinical study for recombinant human endostatin combined with total central radiotherapy for recurrent medulloblastoma in children

Prospective clinical study for recombinant human endostatin combined with total central radiotherapy for recurrent medulloblastoma in children

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023714
Enrollment
Unknown
Registered
2019-06-08
Start date
2019-06-05
Completion date
Unknown
Last updated
2019-06-11

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

Conditions

Medulloblastoma

Interventions

Case series:endostar plus radiotherapy

Sponsors

Army Characteristic Medical Center (Daping Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 6 -18 years old; 2. KPS score (=60); 3. Children with recurrent medulloblastoma (WHO IV grade) confirmed by imaging examination or pathological examination had complete molecular pathological results and recepted surgical resection; 4. Leukocyte count (=4.0 *10^9/L) and platelet count (=100 *10^9/L); 5. Blood urea nitrogen and creatinine < 1.5 times value of the upper limit of normal laboratory; 6. Blood total bilirubin and direct bilirubin < 1.5 times value of the upper limit of normal laboratory; 7. ALT and AST < 1.5 times value of the upper limit of normal laboratory; 8. Patients who were previously healthy and had no serious allergic reaction to biological agents;Patients or their legal guardians voluntarily participate in the group with good compliance, and cooperate with the experimental observation and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. patients who have received other antiangiogenic drugs recently; 2. Patients with severe compression of brainstem, hydrocephalus and other nervous system diseases, which need urgent treatment; 3. Patients with acute or chronic infectious diseases or infectious diseases; 4. Patients with original heart disease, cardiac insufficiency or abnormal electrocardiogram; 5. Patients with uncontrollable mental illness, mental disorder and poor compliance; 6. Patients who can not receive enhanced magnetic resonance scans; 7. Patients who also participated in other clinical trials; 8. patients who researchers believe that should not participate in the trial,such as having active bleeding.

Design outcomes

Primary

MeasureTime frame
Curative effect evaluation;

Countries

China

Contacts

Public ContactGeng Mingying

Army Characteristic Medical Center (Daping Hospital)

m15261891639@163.com+86 023 68811229

Outcome results

None listed

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