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Neoplasm Metastases clinical trials

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NCT ID: NCT02953756 Completed - Neoplasm Metastases Clinical Trials

Cognitive Outcome After Gamma Knife Radiosurgery in Patients With Brain Metastases (CAR-Study A)

Start date: October 2015
Phase:
Study type: Observational

Stereotactic radiosurgery (SRS) is increasingly applied in patients with brain metastases (BM) and is expected to have less adverse effects on cognitive functioning than Whole Brain Radiation Therapy (WBRT). Because cognitive functions are essential for daily functioning, and may affect therapy compliance and quality of life in general, a full understanding of cognitive functioning in patients with BM after SRS is essential. CAR-Study A is a prospective study to evaluate cognitive functioning in patients with 1-10 BM accepted for treatment with Gamma Knife radiosurgery (GKRS).

NCT ID: NCT02808416 Completed - Brain Cancer Clinical Trials

Personalized Cellular Vaccine for Brain Metastases (PERCELLVAC3)

PerCellVac3
Start date: March 1, 2016
Phase: Phase 1
Study type: Interventional

Cancer patients with brain metastases (BM) have poor prognosis. Current treatments produce limited efficacy. Recent advance in cancer immunotherapy has provided important new means to treat cancer patients at advanced stages. This study is designed to perform a clinical trial to treat advanced caner patients with brain metastases with personalized dendritic cell-based cellular vaccines. The patients will receive vaccines consisting of mRNA tumor antigen pulsed DCs. Immune response to the immunized tumor antigens will be monitored. Safety and efficacy will be observed in this study.

NCT ID: NCT02382653 Completed - Neoplasm Metastases Clinical Trials

Oral Piroxicam Versus Buccal Fentanyl in Breakthrough Pain

Start date: December 2014
Phase: N/A
Study type: Interventional

100 patients with Breakthrough pain will be allocated to receive either oral prioxicam (OP) (n=50) or sublingual fentanyl (SLF) (n=50) . Patients will be divided randomly into two equal groups: oral prioxicam (OP) Group and sublingual fentanyl citrate (SLF) Group, comprising of 50 patients each. Pain intensity level on a 0-10 visual analog scale (VAS), patients will be instructed about the use of a 10-cm visual analog scale (VAS) (0 = no pain to 10 = worst possible pain). frequency of Breakthrough pain throughout the day, onset of relief (0-5, 6-10, 11-15, or over 16 min), time required for dose titration, patient satisfaction and adverse effects were assessed at 3, 7, 15, and 30 days after starting the treatment.

NCT ID: NCT01273493 Completed - Clinical trials for Hepatic Insufficiency

A Pharmacokinetic Study of Trabectedin in Patients With Advanced Malignancies and Hepatic Dysfunction

Start date: December 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to characterize the pharmacokinetics (blood levels) of trabectedin after administration to patients with advanced malignancies and hepatic (liver) dysfunction.

NCT ID: NCT01273480 Completed - Neoplasm Metastases Clinical Trials

A Study to Assess the Potential Effects of Rifampin on the Pharmacokinetics of Trabectedin in Patients With Advanced Malignancies

Start date: December 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the potential effects of rifampin on blood levels of trabectedin after administration to patients with advanced malignancies.

NCT ID: NCT01267084 Completed - Neoplasm Metastases Clinical Trials

A Study to Assess the Potential Effects of Ketoconazole on the Pharmacokinetics of Trabectedin in Patients With Advanced Malignancies

Start date: February 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the potential effects of ketoconazole on blood levels of trabectedin after administration to patients with advanced malignancies.

NCT ID: NCT01122199 Completed - Neoplasm Metastases Clinical Trials

Study of RAD001 + AMG479 for Patients With Advanced Solid Tumors

Start date: May 14, 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety of the combination of two drugs called RAD001 and AMG479. This study will see what effects (good and bad) RAD001 and AMG479 have on cancer. This study will also find the highest doses of RAD001 and AMG479 that can be given without causing severe side effects.

NCT ID: NCT00668382 Completed - Neoplasm Metastases Clinical Trials

Evaluate The Toxicity And Feasibility Of Intra-Tumoral Injection

Start date: July 2007
Phase: Phase 1
Study type: Interventional

This is a Phase I pilot study to evaluate the toxicity and feasibility of intratumoral injection (Glycosphingolipids) GSL alpha-GAL (beta-galactosidase) in patients with advanced, refractory solid tumors who have failed standard therapies or are not eligible for standard treatment.

NCT ID: NCT00556049 Completed - Clinical trials for Renal Cell Carcinoma

Combination Sunitinib and Gemcitabine in Sarcomatoid and/or Poor-risk Patients With Metastatic Renal Cell Carcinoma

Start date: December 2007
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to determine if the combination of sunitinib and gemcitabine is effective in treating patients with metastatic renal cell carcinoma. The safety of this combination will also be studied. Sunitinib is approved by the FDA for the treatment of renal cell carcinoma. However, some patients' cancers do not respond to treatment or stops responding after initially responding. Gemcitabine is a chemotherapy drug that is approved by the FDA for the treatment of pancreatic cancer and several other cancers. It is not approved for the treatment of renal cell carcinoma. Previous research has suggested that combining gemcitabine with sunitinib may have some effectiveness in treating metastatic renal cell carcinoma.

NCT ID: NCT00184353 Completed - Neoplasm Metastases Clinical Trials

Clinical MR Spectroscopy of Brain Metastases at 1,5T and 3T.

Start date: November 2003
Phase: N/A
Study type: Observational

Increasing magnetic field is known to give improvements in signal-to-noise-ratio (SNR) and spectral resolution. To investigate this, spectra from different subjects were examined using two clinical MR instruments operating at 1.5T and 3T respectively.