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Clinical research of platinum (cisplatin / carboplatin) combined with dose-dense temozolomide for recurrent malignant glioma

Platinum (cisplatin / carboplatin) combined with dose-dense temozolomide for recurrent malignant glioma: A single-arm, randomized and open lable study

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-14005508
Enrollment
Unknown
Registered
2014-11-18
Start date
2014-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

high-grade glioma

Interventions

Sponsors

First Hospital of Jilin University Department of Radiation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients who meet the following criteria will be eligible for study entry: 1) Patients who had received operation, and had a histopathological diagnosis of malignant glioma; 2) Patients who had received the treatment of standard regimen with radiotherapy with concomitant and adjuvant temozolomide; 3) Patients who had been diagnosed as recurrent malignant glioma confirmed by imaging and pathology; 4) Male and female patients aged between 18 and 70 years; 5) KPS more than 40; 6) No obvious blood routine and biochemical abnormalities confirmed by laboratory examination; 7) No other severe chronic diseases.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: The following patients will be excluded from the study: 1) Pseudo progress can not be excluded according to the clinical manifestations combined with the imaging findings or dynamic recheck; 2) The presence of leptomeningeal metastasis confirmed by imaging findings or cerebrospinal fluid cytological examination; 3) Patients who had the history of severe nervous system disease, or accompanied with severe neurocognitive dysfunction; 4) Patients with poor compliance, or for other reasons, the researchers considered unsuitable to participate in this clinical study;

Design outcomes

Primary

MeasureTime frame
overall survival;therapeutic response;

Secondary

MeasureTime frame
adverse reaction;

Countries

China

Contacts

Public ContactLihua Dong
drlhdong@163.com+86 15843073216

Outcome results

None listed

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