Brain Tumor, Primary

13

Review clinical trials related to Brain Tumor, Primary. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Oral Capecitabine and Temozolomide (CAPTEM) for Newly Diagnosed GBM

The purpose of this study is to evaluate the safety and efficacy of administering the medication capecitabine along with temozolomide when you start your monthly regimen of oral temozolomide for the treatment of your newly diagnosed glioblastoma multiforme (GBM). Capecitabine is an oral chemotherapy that is given to patients with other types of cancer. The study will evaluate whether the dosage of 1500 mg/m2 of capecitabine is tolerable after radiation, when taken along with temozolomide. It will also try to determine if the medication capecitabine helps patients respond to treatment for a longer period of time compared to just temozolomide alone, which is the standard of care.

Participants needed: 67
Trial details
Phase: Phase 1, Phase 2Age: 18-74Biological sex: AllType: InterventionalSponsor: Northwell HealthUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Be capable of giving informed consent. [+9]

Prior chemotherapy with capecitabine or temozolomide for other prior malignancie... [+12]

Status: Not yet recruiting

Evaluating Biomarkers of Cognitive Dysfunction in Patients With Cancer

This study investigates the effects of brain radiotherapy on cognitive function by evaluating plasma biomarkers and apolipoprotein E (APOE) genotype in patients with primary or metastatic brain tumors. Standard brain radiotherapy is known to impact cognitive outcomes, yet the underlying biological mechanisms remain unclear.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of California, San FranciscoUpdated: May 22, 2026Locations: 1
Eligibility criteria

>= 18 years old [+7]

Diagnosis of neurodegenerative disease (Alzheimer's disease, Parkinson's disease... [+2]

Status: Recruiting

Registry of Patients With Brain Tumors Treated With STaRT (GammaTiles)

The objectives of this registry study are to evaluate real-world clinical outcomes and patient reported outcomes that measure the effectiveness and safety of STaRT.

Participants needed: 600
Trial details
Biological sex: AllType: ObservationalSponsor: GT Medical Technologies, Inc.Updated: Feb 13, 2026Locations: 54Duration: 5 Years
Eligibility criteria

Patients who undergo maximum safe resection of intracranial neoplasm(s) AND impl... [+1]

Inability to undergo pre-operative and post-operative imaging for disease and im... [+2]

Status: Not yet recruiting

Correlation Between Nutritional Status of Childhood Neurological Tumors and Quality of Life

Maintaining good nutritional status during treatment for children with cancer is crucial for many outcomes, such as overall survival rate, tolerance to treatment, susceptibility to infection, and quality of life. Neurotumors in children account for the highest proportion among solid tumors in children. Previous studies have clearly shown that neurotumors in children have different nutritional characteristics from hematological tumors and other solid tumors in children. Our retrospective data found that there was a significant correlation between the BMI Z values of children with neurotumors before and during radiotherapy and the frequency of adverse events. The occurrence of adverse events has a negative impact on the quality of life of child patients. Therefore, we plan to conduct a prospective, observational, multi-center longitudinal cohort study to evaluate the dynamic changes in nutritional status during the peri-radiotherapy period, explore the correlation between nutritional status and quality of life in children with neurotumors before and after radiotherapy, and establish a nutritional management plan and nutritional risk early warning model suitable for Chinese children with neurotumors.

Participants needed: 93
Trial details
Age: 5-18Biological sex: AllType: ObservationalSponsor: Nanfang Hospital, Southern Medical UniversityUpdated: Dec 16, 2025
Eligibility criteria

The patient and the legal guardian have agreed to sign the informed consent form... [+4]

Accompanied by other serious complications; [+1]

Status: Recruiting

Circulating Biomarkers Repository in Adults Diagnosed With Primary and Metastatic Brain Tumors

The purpose of this protocol is to create a repository of blood samples from patients diagnosed with primary and metastatic brain tumors who are being seen in the Department of Radiation Oncology at Duke Cancer Center.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Duke UniversityUpdated: Nov 19, 2025Locations: 1
Eligibility criteria

Have a confirmed diagnosis of primary or metastatic brain tumor (histology or im...

None

Status: Recruiting

Focused Ultrasound Blood-Brain Barrier Disruption for the Treatment of High-Grade Glioma in Patients Undergoing Standard Chemotherapy

The goal of this clinical trial is to evaluate the safety and feasibility of focused ultrasound (FUS)-mediated blood-brain barrier (BBB) disruption using the Next Generation Dome Helmet (NGDH) in adults with glioblastoma (GBM) undergoing the maintenance phase of the standard "Stupp protocol". Participants will: * Undergo repeated FUS BBB disruption treatments during the maintenance phase of temozolomide (TMZ) chemotherapy. * Receive intravenous ultrasound contrast (DEFINITY®) prior to each FUS session to facilitate targeted BBB disruption. * Undergo serial MRI scans and clinical assessments to evaluate safety and the extent of BBB opening. * Provide blood samples (and tumor tissue if available) for biomarker analysis related to BBB permeability, tumor presence, and treatment response. * Be followed for progression-free survival (PFS) and overall survival (OS) during routine neuro-oncology visits until end of life.

Participants needed: 10
Trial details
Phase: Phase 1Age: 18-85Biological sex: AllType: InterventionalSponsor: Sunnybrook Health Sciences CentreUpdated: Sep 17, 2025Locations: 1
Eligibility criteria

Age between 18 and 85 years, inclusive. [+7]

The subject presents with symptoms and signs of increased intracranial pressure... [+28]

Status: Recruiting

Radiation Induced Alterations in Resting State Brain Networks in Pediatric Brain Tumor Patients

With modern therapy, the survival rate for pediatric brain tumor patients has significantly improved, with over 70% of patients surviving their disease. However, this progress often comes at the cost of substantial morbidity, with cognitive deficits being the primary obstacle to independent living. Robust predictors of cognitive decline and a comprehensive understanding of the underlying mechanisms of cognitive injury remain elusive. This study will prospectively investigate alterations in brain resting state networks following radiation therapy using functional imaging. The hypothesis is that radiation therapy leads to dose-dependent alterations in functional connectivity in the networks associated with higher level cognition, ultimately leading to cognitive decline.

Participants needed: 16
Trial details
Age: 8-21Biological sex: AllType: ObservationalSponsor: Washington University School of MedicineUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Between 8 and 21 years of age, inclusive [+3]

Presence of visual impairment to an extent that the patient is unable to complet... [+3]

Status: Not yet recruiting

3D Decision Support Tool for Brain Tumour Surgery Development and Validation: Observational Study

This observational study (STRATUM-OS) aims to collect the necessary data from a cohort of patients with planned surgery for suspected intra-axial malignant brain tumours (both primary and secondary) following the standard surgical procedure established in current clinical protocols. These data will serve two primary purposes: i) To gather multimodal data (pre, intra and postoperative) essential for the development and technical validation of a 3D decision support tool for brain surgery guidance and diagnostics integrating augmented reality and multimodal data processing powered by artificial intelligence algorithms (called STRATUM tool); ii) To collect outcome measures that will facilitate a subsequent comparative study (a non-randomized controlled clinical trial, called STRATUM-NRCCT) assessing the standard procedure alone versus the standard procedure augmented with the STRATUM tool. Patients from STRATUM-OS will act as a historical control group in the subsequent historically controlled clinical trial (STRATUM-NRCCT), which will be performed once STRATUM-OS has been completed. In STRATUM-OS patients will receive standard care as per established clinical protocols, with no modification to their treatment. However, patients will be asked to grant access to their clinical information, complete questionnaires, and provide relevant pre, intra and postoperative information related to the surgical intervention. Data will be gathered from multiple sources, such as the Electronic Health Records (EHR), patient completed questionnaires, interviews, and reports from healthcare professionals involved in the surgical procedure. Additionally, intraoperative data will be collected from the different devices in the operating room.

Participants needed: 320
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fundación Canaria Instituto de Investigación Sanitaria de CanariasUpdated: Jun 25, 2025Duration: 6 Months
Eligibility criteria

Adult patients (≥18 y/o). [+1]

Inability to deliver informed consent (unless provided by the tutor). [+1]

Status: Recruiting

Characterization of Circulating and Tumor-infiltrating Immune Cells in Malignant Brain Tumors

The goal of this observational study is to characterize the circulating leukocyte profile and the immune T cells distribution within the tumor in patients with malignant brain tumors and to correlate these findings with the oncological outcome. Participants will be subjected to blood sampling before surgery and for 12 months of follow-up. Additional sampling and analysis will be performed on tumor samples.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Pietro Mortini, MD, Prof.Updated: Jun 11, 2025Locations: 1
Eligibility criteria

Adult patients (≥18 years) [+3]

Patients who do not meet inclusion criteria.

Status: Recruiting

Glutamate Excitotoxicity and Its Role in Glioblastoma Biology

Gliomas are the most frequent type of primary brain tumors in adults; among them glioblastoma multiforme (GBM) is the most malignant, being associated with the worst prognosis. Glutamate (Glu) is an aminoacid, responsible for essential functions in the Central Nervous System (CNS), acting both as metabolite and neurotransmitter. It is essential for regulating cellular metabolism and developmental synaptogenesis, cellular migration, differentiation and death. Recent scientific evidences have demonstrated alteration in Glu synthesis and signaling being directly involved in GBM growth and invasion

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: IRCCS San RaffaeleUpdated: Jun 11, 2025Locations: 1
Eligibility criteria

Adult patients with a brain lesion suspected for GBM, candidate to gross total t... [+1]

Age < 18 years [+3]

Status: Not yet recruiting

Research on the Safety and Efficacy of Intraoperative Radiation Therapy in Malignant Cerebral Tumor

According to the latest national cancer statistics released by the National Cancer Center in February 2022, intracranial tumors account for about 60%-70% of the more than 3.5 million cancer patients, and the morbidity and mortality remain high. Intracranial malignant tumors have become a problem that needs to be solved urgently because of their early recurrence, rapid progression, and short survival, and intracranial malignant tumors include high-grade gliomas, metastases, lymphomas, etc. Glioblastoma (GB) is the most common primary malignancy in the adult central nervous system, accounting for about 57% of all gliomas and 48% of all primary weighted nervous system malignancies. At present, the standard treatment for glioblastoma is mainly surgical treatment, supplemented by postoperative concurrent chemoradiotherapy and adjuvant chemotherapy, but the prognosis of patients is still poor, with a one-year survival rate of 40.6%, a five-year survival rate of only 5.6%, and an average survival time of 12-15 months. For patients diagnosed with intracranial malignancies (including high-grade glioma, metastases, lymphoma, etc.), multimodal image-guided microsurgery combined with postoperative chemoradiotherapy recommended by the guidelines, and intraoperative radiotherapy with tumor bed radiation therapy to achieve targeted and precise tumor treatment, thereby improving the prognosis of patients (including progression-free survival and median overall survival, etc.)

Participants needed: 200
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: First Affiliated Hospital, Sun Yat-Sen UniversityUpdated: Apr 16, 2025
Eligibility criteria

18-75 years old, non-pregnant or lactating women [+7]

Refuse to undergo craniotomy or radiation therapy; [+2]

Status: Recruiting

FeelFit: High-intensity Interval Training to Improve Self-reported Physical Fitness in Brain Tumor Patients

The FeelFit study aims to assess the effectiveness of High-Intensity Interval Training (HIIT) in improving self-reported physical fitness in adult brain tumor patients during periods of stable disease, as compared to a waiting-list control group. Furthermore, several secondary and exploratory outcomes will be evaluated. The study is part of the GRIP (GuaRding quality survivorshiP) project, which aims to improve quality of life in brain tumor patients.

Participants needed: 36
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Amsterdam UMC, location VUmcUpdated: Apr 6, 2025Locations: 1
Eligibility criteria

reduced self-reported physical fitness; [+5]

Karnofsky Performance Score < 70; [+2]

Status: Recruiting

SeOuL cOhort of Brain Tumor MONitoring Study (SOLOMON)

The registry of this study was subjected to patients who were radiologically diagnosed with a non-malignant brain tumor at Seoul National University Hospital since 2001, and who have had magnetic resonance (MR) re-examination after first MR exam or will be re-examined because it was determined that immediate treatment would not be needed at the first visit to the hospital. In all MRs taken by patients, the date of imaging and the volume of the tumor are measured, and we aim to establish a natural growth history for non-malignant brain tumors.

Participants needed: 3,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Seoul National University HospitalUpdated: Dec 3, 2024Locations: 1Duration: 15 Years
Eligibility criteria

Patients with radiologically diagnosed brain neoplasm of CNS WHO grade 2 or less... [+11]

Patients who lost follow-up before the second MR exam [+2]