Clinical trial Recruiting at 1 site Interventional Ages 18 to 70

Blocking blood supply to treat glioblastoma

Official title: Research on the Safety and Efficacy of Blocking Dural Blood Supply in Glioblastoma Patients

Run by First Affiliated Hospital, Sun Yat-Sen University · NCT05990556 · Data updated 2026-11-12

This study is testing a new procedure that blocks blood flow to glioblastoma tumors to see if it can help the immune system fight the cancer better in people who haven't had treatment yet.

More Glioblastoma trials

Quick facts

Study typeInterventional
Ages18 Years to 70 Years
SexAll
Enrollment20 (estimated)
SponsorFirst Affiliated Hospital, Sun Yat-Sen University
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Guangzhou, Guangdong)
StatusRecruiting
StartedMay 11, 2024
Main results expectedSeptember 1, 2025
Study endsSeptember 1, 2028
Registry record updatedJuly 24, 2024
Trial IDNCT05990556 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are patients with a confirmed diagnosis of glioblastoma who have not received prior treatments.

Probably not a fit

Patients whose glioblastoma diagnosis is later confirmed to be incorrect or those with significant comorbidities affecting survival may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the safety and efficacy of an interventional procedure aimed at blocking the blood supply from the meningeal arteries in patients diagnosed with glioblastoma. The approach is based on the hypothesis that altering the immune microenvironment can enhance the effectiveness of immune responses against the tumor. Eligible participants include those who have not undergone prior treatments for their glioblastoma, allowing for a clearer assessment of the intervention's impact. The study aims to provide insights into how manipulating blood supply can influence tumor progression and immune activation.

Why it matters

Potential benefit: If successful, this approach could lead to improved treatment outcomes for glioblastoma patients by enhancing immune responses against the tumor.

How similar studies have gone: While there is ongoing research into the immune microenvironment of glioblastoma, this specific approach of blocking meningeal blood supply is novel and has not been extensively tested in prior studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Imaging or needle biopsy pathologically diagnosed as glioblastoma
* Patients have not previously received radiotherapy, chemotherapy and other treatment modalities for intracranial lesions
* There are no related contraindications such as neurovascular intervention and craniotomy

Exclusion Criteria:

* The patient's initial imaging diagnosis was glioblastoma, and the postoperative pathology confirmed nonglioblastoma
* The patient has other underlying medical conditions that affect survival time
* The patient had other underlying medical conditions that affected follow-up or quality of life assessment
* Patients do not have the above exclusion criteria and refuse to participate in clinical trials after informed consent

Where it's running

  • the First Affiliated Hospital of Sun Yat-sen University
    Guangzhou, Guangdong, China
    Recruiting

Study contacts

  • Principal investigator: Nu Zhang, Professor — First Affiliated Hospital, Sun Yat-Sen University
  • Study coordinator: Nu Zhang, Professor
  • Email: zhangnu2@mail.sysu.edu.cn
  • Phone: 13825070717

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.