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Brain Neoplasm clinical trials

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NCT ID: NCT01413438 Withdrawn - Glioblastoma Clinical Trials

Bevacizumab With or Without Surgery for Adult Glioblastomas

Start date: July 15, 2011
Phase: Phase 2
Study type: Interventional

Background: - Glioblastoma (GBM) is the most common malignant brain tumor in adults. Patients with GBM are usually treated with surgery, radiation, and chemotherapy. Despite this treatment, most GBMs start growing again. Bevacizumab, a chemotherapy drug, has shown promise in slowing the growth of GBMs. More research is needed to find out whether having surgery before starting bevacizumab is more effective than bevacizumab alone. Objectives: - To compare surgery plus bevacizumab to bevacizumab alone in adults with glioblastoma. Eligibility: - Individuals at least 18 years old whose glioblastoma has come back after treatment. Design: - All participants will be screened with a physical exam, medical history, blood tests, and imaging studies. - Participants will be divided into two groups. One group will have surgery followed by bevacizumab. The other group will have the drug without surgery. - The first group will have surgery as soon as possible and will begin bevacizumab 4 weeks after surgery. The second group will start the drug as soon as possible. - Both groups will receive the drug as an infusion every 2 weeks. They will be monitored with frequent blood tests and imaging studies. The infusions will continue for as long as the drug is effective at preventing tumor regrowth. - Participants will be contacted every 4 weeks after they stop taking bevacizumab. They will answer followup questions either in person or by telephone.

NCT ID: NCT01124461 Completed - Clinical trials for GLIOBLASTOMA MULTIFORME

BIRN (Biomedical Informatics Research Network) Resources Facilitate the Personalization of Malignant Brain Tumor

CONDR
Start date: January 2010
Phase:
Study type: Observational

The goal of this study is to create a comprehensive database of Magnetic Resonance Imaging (MRI) and of pathology for patients with brain tumors. Both standard, advanced, and research MRI components may be included, these will be analyzed in comparison with pathology results if/when a biopsy is obtained, and also used to predict/evaluate responses to therapy. This study will create a database of de-identified MRI images which include these techniques so that brain tumors can be studied over time (longitudinally) in an organized manner.

NCT ID: NCT00880061 Terminated - Glioma Clinical Trials

An Open Label Dose Escalation Safety Study of Convection-Enhanced Delivery of IL13-PE38QQR in Patients With Progressive Pediatric Diffuse Infiltrating Brainstem Glioma and Supratentorial High-grade Glioma

Start date: April 7, 2009
Phase: Phase 1
Study type: Interventional

Background: - Diffusely infiltrating pontine glioma (DIPG) or supratentorial high-grade glioma (HGG) are brain tumors that are often difficult to treat. It is very difficult to get chemotherapy agents to tumors in the brain, and researchers are looking for new methods to directly treat these types of cancer. - IL-13 is an immune molecule normally occurring in the body. Patients with gliomas appear to have significant amounts of the IL-13 receptors in their brain tumors. An experimental drug, IL13-PE38QQR, combines a bacteria toxin with human IL-13 to allow the toxin to enter and destroy the tumor cell. Early clinical studies suggest this treatment may prolong survival of patients with these types of brain tumors. - A technique called convection-enhanced delivery (CED) uses continuous pressure to push large molecules through the membranes protecting the brain to reach brain tumors. This technique can treat a tumor more directly than with traditional methods. Objectives: - To test the safety and feasibility of giving IL13-PE38QQR directly into regions of the brain in pediatric patients with DIPG or HGG, using CED. - To determine the most appropriate dose of IL13-PE38QQR to treat DIPG or HGG. - To determine the effects of this experimental therapy on the tumor. - To evaluate the physical changes in the tumor before and after the therapy. Eligibility: - Patients who are less than 18 years of age and have been diagnosed with either DIPG or with supratentorial HGG that has not responded well to standard treatments. Design: - Patients will be admitted to the hospital and will receive a magnetic resonance imaging (MRI) scan to show the exact location of the tumor. A small plastic tube will be inserted surgically into the tumor area, and IL13-PE38QQR and a MRI contrast agent (gadolinium DTPA) will be infused into the area. - MRI scans will monitor the process, and the tube will be removed after surgery. - Doses will be adjusted over the course of the study. - Patients who respond well to treatment may be eligible to receive a second infusion, no sooner than 4 weeks after the first treatment. - Post-treatment visits: Clinic visits 4 and 8 weeks after the treatment, and then every 8 weeks for up to 1 year. - Physical examination with neurological testing, an MRI, and standard blood and urine tests.

NCT ID: NCT00747253 Completed - Clinical trials for Glioblastoma Multiforme

Monteris AutoLITTâ„¢ FIM Safety Trial for Recurrent/Progressive Brain Tumors

Start date: August 2008
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to evaluate the safety and performance of the AutoLITT system for the treatment of recurrent/progressive glioblastoma multiforme tumors (GBM).

NCT ID: NCT00638963 Terminated - Breast Neoplasm Clinical Trials

Temozolomide as a Prophylaxis Against Brain Recurrence in Participants With Metastatic Breast Cancer (P05225 AM2)

STOP
Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether temozolomide can be used as a prophylaxis against brain recurrence in participants with metastatic breast cancer.

NCT ID: NCT00199511 Completed - Brain Tumor Clinical Trials

Hypertonic Saline 75% vs Mannitol 20%

Start date: January 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of Hypertonic Saline 7.5% vs Mannitol 20% on brain bulk (using a 4 point scale), intracranial pressure (subdural catheter)and the changes on serum and urinary Na, K and Osmolarity during elective craniotomy for brain tumor resection.

NCT ID: NCT00178295 Completed - Brain Neoplasm Clinical Trials

Radiation-Induced Cytokine Cascades and Their Correlation With Central Nervous System Injury

Start date: November 1999
Phase: N/A
Study type: Observational

Treatment for brain cancer may include radiation therapy. Radiation therapy is the treatment of tumors with X-rays. This study is related to understanding the side effects of radiation treatment for brain tumors. This study is being conducted by the University of Rochester Cancer Center to compare the extent of side effects of brain cancer treatment with changes in levels of blood proteins called cytokines.

NCT ID: NCT00124761 Completed - Neoplasm Metastasis Clinical Trials

A Trial Comparing Radiosurgery With Surgery for Solitary Brain Metastases

Start date: December 2002
Phase: Phase 3
Study type: Interventional

This study examines surgery versus radiosurgery (highly focussed radiation) for the treatment of cancer which has spread to one spot in the brain (solitary brain "metastasis"). For these two treatment options, it will compare patients' survival times, quality of life, control rate of the brain metastases and side effects. It uses the most rigorous scientific method available called "randomisation" which minimises biases that exist with other types of studies. It will involve 30 - 40 patients.

NCT ID: NCT00080054 Completed - Glioblastoma Clinical Trials

A Study of Motexafin Gadolinium and Temozolomide for the Treatment of Malignant Gliomas

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out about the safety of adding the investigational drug motexafin gadolinium to a standard course of chemotherapy with temozolomide for patients with malignant glioma. Secondly, the study will determine how many patients will respond to this treatment.

NCT ID: NCT00042445 Completed - Leukemia Clinical Trials

Brain Neoplasms, Leukemia and Petrochemical Exposures

Start date: August 2000
Phase: N/A
Study type: Observational

The aim of this study is to examine the association of exposure to air contaminants (PAH & VOC) emitted from the petrochemical industries, specific genetic polymorphisms (P4501A1 (MspI & exon 7) and GSTM1 & T1) of study subjects and their parents, and the risks of brain tumors and leukemia among children and youths in metropolitan Kaohsiung, southern Taiwan.