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Study on the clinical benefits of reoperation in patients with recurrent glioblastoma

Study on the clinical benefits of reoperation in patients with recurrent glioblastoma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034017
Enrollment
Unknown
Registered
2020-06-21
Start date
2020-06-20
Completion date
Unknown
Last updated
2020-06-22

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

Conditions

Glioblastoma

Interventions

Surgical group:Maximum range of brain tumor resection +/ chemotherapy (temozolomide/bevacizumab)+/ radiotherapy + adjuvant therapy
Surgical only group:Maximum range of brain tumor resection +adjuvant therapy
Non-surgical group:Chemotherapy (temozolomide/bevacizumab)+/ radiotherapy + adjuvant therapy
Chemotherapy only group:Chemotherapy (temozolomide/bevacizumab)+ adjuvant therapy

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. The first postoperative pathological diagnosis was glioblastoma; 3. Brain MRI (plain scan + enhancement) should be reviewed every 3 months after discharge, or brain MRI should recur in time when symptoms, such as progressive headache, weakness or neurological symptoms, are present, so as to determine the time of recurrence; 4. Diagnosed as postoperative recurrence of glioblastoma after multidisciplinary consultation, or pathologically diagnosed as postoperative recurrence of glioblastoma after the second postoperative diagnosis; 5. Able to understand and willing to sign the informed consent; Ability and willingness to follow study and follow-up procedures.

Exclusion criteria

Exclusion criteria: 1. Patients with other malignant tumors; 2. The first operation was biopsy surgery; 3. The patient did not review MRI (plain scan + enhancement) within 24-72 hours after the first operation, so the degree of resection could not be accurately determined 4. The patient was unable to accurately determine the time of recurrence due to the lack of reexamination MRI data after the first operation; 5. The patient did not receive standard chemoradiotherapy after the first operation; 6. Severe uncontrolled infection or medical problems.

Design outcomes

Primary

MeasureTime frame
Progressive epigenetic lifetime;overall survival;progression-free survival;quality of life;Brain MRI;

Countries

China

Contacts

Public ContactZhiqiang Li

Zhongnan Hospital of Wuhan University,

lifenzhi@163.com+86 18907123005

Outcome results

None listed

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