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Neoplasms clinical trials

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NCT ID: NCT01808625 Terminated - Clinical trials for BRAIN MALIGNANCIES AFTER RADIATION THERAPY

Hyperbaric Oxygen Stimulation for Patients With Brain Malignancies After Radiation Therapy.

Start date: March 2013
Phase: N/A
Study type: Interventional

Radiotherapy is the mainstay of treatment for brain malignancies and is associated with significant neurotoxicity. Due to continuous increase in patient's survival, the long term risk for radiation-induced brain inflammation and necrosis inducing secondary cognitive impairments are increasing concerns. Currently there is no effective treatment for preventing long term radiation-induced brain damage. Hyperbaric oxygen therapy (HBOT) is the administration of high oxygen concentrations within a pressurized chamber to increase the cellular/mitochondrial delivery of oxygen. Oxygen stimulation by HBOT has become the definitive therapy for radiation-induced damage to soft tissues and bone due to its ability to stimulate healing processes by supplying the energy/oxygen needed while down-regulating genes involved in inflammation. Oxygen stimulation by HBOT is currently indicated for patients with overt radiation-induced neurotoxicity and was proven to reduce further development of radiation damage while stimulating "idling" neurons to return to function. Since HBOT is considered safe, we hypothesize that its application following radiation, before the manifestation of neurological side effects, may help avert development of early/delayed onset radiation-induced neurotoxicity. In the proposed study, for the first time, HBOT will be applied early after radiation to prevent the expected decrease in patients neurocognitive functions (NCF) and improve their quality of life (QOL). The study is designed to provide statistically significant assessment, in a prospective randomized clinical trial, of the effect of oxygen stimulation applied soon after brain radiotherapy, for patients with primary and secondary brain tumors, on patients QOL and NCF. In addition, advanced imaging methodologies will be applied to study the feasibility of quantifying oxygen stimulation effects on the tumor and surrounding brain tissue.

NCT ID: NCT01808534 Terminated - Clinical trials for Recurrent Ovarian Germ Cell Tumor

Palifosfamide in Treating Patients With Recurrent Germ Cell Tumors

Start date: February 2013
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well palifosfamide works in treating patients with recurrent germ cell tumors. Drugs used in chemotherapy, such as palifosfamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing

NCT ID: NCT01808079 Completed - Clinical trials for Stage III Kidney Wilms Tumor

Gene Analysis in Studying Susceptibility to Wilms Tumor

Start date: October 2009
Phase: N/A
Study type: Observational

This clinical trial studies gene analysis in studying susceptibility to Wilms tumor. Finding genetic markers for Wilms tumor may help identify patients who are at risk of relapse.

NCT ID: NCT01806129 Active, not recruiting - Malignant Neoplasm Clinical Trials

Reproductive Health Program in Patients With Cancer

EROS
Start date: September 2, 2016
Phase: N/A
Study type: Interventional

This clinical trial studies reproductive health program in patients with cancer. A reproductive health program may improve patients' understanding of reproductive risks and receipt of appropriate treatment to achieve their reproductive health goals.

NCT ID: NCT01804634 Recruiting - Clinical trials for Refractory and/or Relapsed Metastatic Solid Tumors

Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Start date: March 27, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if giving reduced intensity chemotherapy, haploidentical bone marrow, post-transplant cyclophosphamide and shortened duration tacrolimus is safe and feasible for patients with very high-risk solid tumors.

NCT ID: NCT01804530 Terminated - Solid Tumor Clinical Trials

Phase 1 Study of PLX7486 as Single Agent in Patients With Advanced Solid Tumors

Start date: August 2013
Phase: Phase 1
Study type: Interventional

The objective of this study is to determine the safety, pharmacokinetics, maximum tolerated dose/recommended Phase 2 dose, and efficacy of PLX7486.

NCT ID: NCT01802996 Recruiting - Neoplasms Clinical Trials

Evaluate the Efficacy of Magnesium Isoglycyrrhizinate in the Prevention of Chemotherapy Related Acute Liver Injury

MAGIC
Start date: March 2013
Phase: Phase 4
Study type: Interventional

This purpose of this study is to evaluate the evaluate the efficacy of Magnesium Isoglycyrrhizinate Injection in the prevention of antineoplastic chemotherapy related acute liver injury.

NCT ID: NCT01802203 Completed - Barrett Esophagus Clinical Trials

trÅ«Freeze® Spray Cryotherapy Patient Registry

Start date: April 2013
Phase:
Study type: Observational [Patient Registry]

To collect efficacy and outcomes data related to the use of trÅ«Freeze® spray cryotherapy for the treatment of unwanted tissue in the pulmonary and gastrointestinal settings.

NCT ID: NCT01800630 Completed - Clinical trials for Advanced Solid Malignancies

Phase1 Study of Gemcitabine HCl Oral Formulation(D07001-F4) in Patients With Advanced Solid Malignancies and Malignant Lymphomas

Start date: April 2013
Phase: Phase 1
Study type: Interventional

Open-label Phase 1 sequential dose-escalation study of 10 increasing doses (3 to 6 patients each)to determine and characterize the DLTs and MTD of gemcitabine HCl oral formulation (D07001-F4). Patients will be assigned to receive oral D07001-F4 on Days 1, 3, 5, 8, 10, and 12 of 4 21-day cycles each to further characterize safety and tolerability.

NCT ID: NCT01798771 Not yet recruiting - Glioblastoma Clinical Trials

Intraoperative MRI and 5-ALA Guidance to Improve the Extent of Resection in Brain Tumor Surgery

IMAGER
Start date: March 2013
Phase: N/A
Study type: Interventional

The investigators hypothesize that the rate of radiologically complete resections of contrast-enhancing brain tumors following surgeries aided by use of 5-ALA induced fluorescence guidance and use of an intraoperative ultra-low field MRI is higher compared to surgeries aided by 5-ALA induced fluorescene alone.