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Neoplasms clinical trials

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NCT ID: NCT00189410 Completed - Cervical Cancers Clinical Trials

Combination Chemotherapy Consisting of Pegylated Liposomal Doxorubicin and Carboplatin in Malignant Gynecologic Tumours

Start date: June 2003
Phase: Phase 2
Study type: Interventional

Pegylated Liposomal Doxorubicin as well as Carboplatin have been showed efficacy in monotherapy as in combination therapy of gynaecologic tumours. As there is no common standard in the therapy of recurrent ovarian carcinoma, tumours of the uterus nor for non-epithelial ovarian tumours at time of designing of this study, this trial shall evaluate the new and well tolerated combination therapy consisting of Pegylated Liposomal Doxorubicin and Carboplatin.

NCT ID: NCT00189345 Completed - Ovarian Cancer Clinical Trials

Randomized, Multicenter, 2-Dose Level. Open-Label, Phase IIa Study With the Intraperitoneally Infused Trifunctional Bispecific Antibody Removab(TM) (Anti-EpCAM x Anti-CD3) to Select the Better Dose Level in Platinum Refractory Epithelial Ovarian Cancer Patients

Start date: May 2004
Phase: Phase 2
Study type: Interventional

Patients with epithelial ovarian cancer, fallopian tube or peritoneal cancer who receive surgical cytoreduction and platinum/taxane containing chemotherapy have a significant chance of entering complete clinical remission but about 70% will eventually relapse. Many patients respond to additional cytotoxic treatment with partial or complete responses, yet approximately 100% of these patients will ultimately progress. Novel consolidation strategies following treatment for recurrent disease are needed and an immunologic approach is an attractive option.EpCAM is expressed in a large number of epithelial ovarian cancer, fallopian tube or peritoneal cancer tissues. Thus targeting these cancers with an anti-EpCAM antibody is a promising innovative therapeutic approach.

NCT ID: NCT00188695 Completed - Prostatic Neoplasms Clinical Trials

Combidex USPIO - Ultra-small Superparamagnetic Iron Oxide

Start date: April 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test whether or not a new contrast agent called Combidex, a contrast agent formulated from ultra-small superparamagnetic iron oxide (USPIO) improves the ability of Magnetic Resonance Imaging (MRI) to see lymph nodes in the pelvis. It might also help doctors tell whether or not cancer has spread to these lymph nodes. It might allow radiotherapy to be delivered more accurately.

NCT ID: NCT00188578 Completed - Uterine Neoplasms Clinical Trials

Intensity Modulated Radiation Therapy - Gyne Cancer (GY03.2)

Start date: June 2003
Phase: Phase 1/Phase 2
Study type: Interventional

Standard treatment for gynecological cancer is radiation therapy in two phases; whole pelvic radiation and then an internal radiation boost, also called a brachytherapy boost, to treat any remaining tumour. The purpose of this study is to test an alternative radiation boost treatment called conformal intensity modulated radiation therapy or IMRT. Currently, we do not have complete information on the overall effectiveness of IMRT compared to brachytherapy or conformal radiotherapy. We know that IMRT allows the radiation beams to be more accurately focused on the tumor, thereby sparing more normal tissue from radiation damage and lowering risks of side effects. We are investigating the extent to which IMRT can be used to protect normal tissues in patients with cervix, uterine or vaginal cancer from the radiation beams and how much the side effects of radiation are reduced.

NCT ID: NCT00187226 Completed - Brain Tumors Clinical Trials

A Study for Image-Guided Radiation Therapy in Pediatric Brain Tumors and Side Effects

Start date: June 1997
Phase: Phase 2
Study type: Interventional

The purpose of the study was to determine if treating a limited volume of normal tissue surrounding the tumor or tumor bed using conformal radiation therapy would achieve similar rates of disease control compared to standard radiation therapy. The study was also conducted to examine the effect of irradiation on neurological, endocrine and cognitive function.

NCT ID: NCT00187174 Completed - Tumors Clinical Trials

Everolimus for Treating Pediatric Patients With Recurrent or Refractory Tumors

Start date: October 2004
Phase: Phase 1
Study type: Interventional

Patients with recurrent or refractory solid tumors or brain tumors that are unresponsive to conventional therapy, or with no known effective therapy, will be treated. Experiments in the laboratory have shown the experimental drug RAD001C (RAD001, Everolimus) can prevent cells from multiplying. RAD001 is now being tested in diseases such as cancer, in which excessive cell multiplication needs to be stopped. The drug has been tested in adult cancer patients and has been well tolerated by subjects in these studies. It is experimental and, therefore, available in clinical trials.

NCT ID: NCT00186953 Completed - Pelvic Neoplasms Clinical Trials

Determination of a Safe Dose of Optison in Pediatric Patients With Solid Tumors

Start date: June 2002
Phase: Phase 1
Study type: Interventional

St. Jude Children's Research Hospital is studying ways to make ultrasound images clearer - to be able to see blood vessels, body structures, and tumors better. Ultrasound uses sound waves to create pictures, allowing doctors and other medical professionals to "see" inside the body. Researchers are studying a contrast agent (like a dye) called Optison™. St. Jude Children's Research Hospital researchers want to learn the best and safest dose of this ultrasound "dye."

NCT ID: NCT00185692 Completed - Leukemia Clinical Trials

Allogeneic Transplantation From Related Haploidentical Donors

Start date: August 2000
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the feasibility and safety of transplanting CD34+ selected hematopoietic cells from a haploidentical related donor following a nonmyeloablative regimen of total lymphoid irradiation (TLI) and antithymocyte globulin (ATG).

NCT ID: NCT00184275 Completed - Melanoma Clinical Trials

Characterization of Brain Metastases

Start date: May 2005
Phase: N/A
Study type: Observational

The purpose is to characterize tumour biological markers in brain metastases tissue from patients with different primary tumour by using ex vivo techniques as high-resolution magic angle spinning MR spectroscopy and micro array.

NCT ID: NCT00179881 Completed - Clinical trials for Neoplasms, Brain Stem

Thalomid and Carboplatin for the Treatment of Pediatric Brain Stem Glioma

Start date: December 1999
Phase: Phase 2
Study type: Interventional

Treatment on this study combines two drugs: Thalomid™ (thalidomide) and carboplatin. Thalidomide has been available for many years and has been used to treat many different illnesses. Carboplatin is an effective medicine in killing cancer cells. Thalidomide works by blocking angiogenesis (the process of new blood vessel formation). If a tumor does not have blood vessels providing oxygen and nutrients, it will not be able to grow. This research will look at how combining the effects of thalidomide (preventing tumor growth) with the tumor killing effect of carboplatin effects the long-term outlook for patients with these tumors. This study will try to find out how well Thalomid™ and carboplatin combined with radiation therapy works in treating children newly diagnosed with brain stem glioma. This study will look at how well Thalomid ™ and carboplatin work in patients with recurrent brain stem glioma. This study will also look at any side effects of these treatments.