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Endometrial Cancer clinical trials

View clinical trials related to Endometrial Cancer.

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NCT ID: NCT00416455 Completed - Clinical trials for Cervical Adenocarcinoma

Fludeoxyglucose (FDG) F 18 PET Scan, CT Scan, and Ferumoxtran-10 MRI Scan Before Chemotherapy and Radiation Therapy in Finding Lymph Node Metastasis in Patients With Locally Advanced Cervical Cancer or High-Risk Endometrial Cancer

Start date: September 2007
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial is studying how well fludeoxyglucose F 18 PET scan, CT scan, and ferumoxtran-10 MRI scan finds lymph node metastasis before undergoing chemotherapy and radiation therapy in patients with locally advanced cervical cancer or high-risk endometrial cancer. Diagnostic procedures, such as a fludeoxyglucose F 18 positron emission tomography (PET) scan, computed tomography (CT) scan, and ferumoxtran-10 magnetic resonance imaging (MRI) scan, may help find lymph node metastasis in patients with cervical cancer or endometrial cancer.

NCT ID: NCT00411138 Active, not recruiting - Endometrial Cancer Clinical Trials

Randomized Trial of Radiation Therapy With or Without Chemotherapy for Endometrial Cancer

PORTEC-3
Start date: November 23, 2006
Phase: Phase 3
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as cisplatin, paclitaxel, and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving chemotherapy and radiation therapy after surgery may kill any tumor cells that remain after surgery. It is not yet known whether giving chemotherapy together with radiation therapy is more effective than giving radiation therapy alone in treating endometrial cancer. PURPOSE: This randomized phase III trial is studying chemotherapy and radiation therapy to see how well they work compared with radiation therapy alone in treating patients with high-risk, stage I, stage II, or stage III endometrial cancer.

NCT ID: NCT00401635 Completed - Endometrial Cancer Clinical Trials

END-1: First Line Chemotherapy for Advanced or Recurrent Endometrial Carcinoma With Carboplatin and Liposomal Doxorubicin

Start date: November 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate activity and toxicity of the combination of carboplatin and liposomal doxorubicin as first-line chemotherapy of patients with advanced or recurrent endometrial carcinoma.

NCT ID: NCT00394602 Terminated - Pancreatic Cancer Clinical Trials

Chemoradiation-Induced Nausea and Emesis: Quality of Life

Start date: April 7, 2004
Phase:
Study type: Observational

The primary objectives of this study are: 1. To assess the preferences of cancer patients scheduled to receive chemoradiation and caregiver controls for side-effects of chemoradiation. 1. To compare preferences of cancer patients to those of healthy individuals. 2. To compare how patients' preferences for side-effects of chemoradiation change over time. 2. To longitudinally assess the quality of life of cancer patients scheduled to receive chemoradiation. 3. To determine the impact of nausea and vomiting associated with chemoradiation on patients' quality of life and evaluate potential change throughout the duration of chemoradiation treatment.

NCT ID: NCT00392769 Completed - Endometrial Cancer Clinical Trials

Cetuximab in Patients With Progressive or Recurrent Endometrial Cancer

Start date: October 2006
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if cetuximab can help to control the disease in patients who have recurrent endometrial cancer. Primary Objective: 1. To determine the overall disease control rate of cetuximab in patients with progressive or recurrent endometrial cancer. Secondary Objectives: 1. To determine the duration of disease control, time to disease progression, and survival of this cohort of patients. 2. To determine the nature and degree of toxicity of cetuximab in this cohort of patients. 3. To correlate biologic markers with response to therapy if tissue is available.

NCT ID: NCT00388154 Completed - Endometrial Cancer Clinical Trials

Gemcitabine and Cisplatin for Advanced or Recurrent Endometrial Cancer

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

Primary Objective: - To estimate the antitumor activity of the combination of gemcitabine and cisplatin in patients with advanced (stage III or IV) or recurrent endometrial cancer. Secondary Objective: - To determine the nature and degree of toxicity of the combination of gemcitabine and cisplatin in this cohort of patients.

NCT ID: NCT00381888 Completed - Ovarian Cancer Clinical Trials

Fondaparinux in Preventing Blood Clots in Patients Undergoing Surgery for Gynecologic Cancer

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

RATIONALE: Fondaparinux may help prevent blood clots from forming in patients who are undergoing surgery for gynecologic cancer. PURPOSE: This phase II trial is studying how well fondaparinux works in preventing blood clots in patients undergoing surgery for gynecologic cancer.

NCT ID: NCT00377520 Completed - Neoplasms Clinical Trials

A Trial for Patients With Advanced/Recurrent Endometrial Cancer

Start date: September 2006
Phase: Phase 2
Study type: Interventional

The intent of this protocol is to screen a new agent for activity in patients with advanced or recurrent endometrial carcinoma. This phase II trial is studying how well pemetrexed disodium works in treating patients with advanced or recurrent endometrial carcinoma.

NCT ID: NCT00376844 Completed - Endometrial Cancer Clinical Trials

External-Beam Radiation Therapy Compared With Vaginal Brachytherapy After Surgery for Stage I Endometrial Cancer

PORTEC-2
Start date: May 2002
Phase: Phase 3
Study type: Interventional

RATIONALE: External-beam radiation therapy uses high-energy x-rays to kill tumor cells. Implant radiation therapy uses radioactive material placed directly into or near a tumor to kill tumor cells. Giving external-beam radiation therapy or implant radiation therapy after surgery may kill any tumor cells that remain after surgery. Sometimes, after surgery, the tumor may not need more treatment until it progresses. In this case, observation may be sufficient. It is not yet known whether radiation therapy is more effective than observation when given after surgery in treating stage I endometrial cancer. PURPOSE: This randomized phase III trial is studying external-beam radiation therapy or implant radiation therapy to see how well they work compared with observation in treating patients who have undergone surgery for stage I endometrial cancer.

NCT ID: NCT00375804 Terminated - Endometrial Cancer Clinical Trials

Racial Disparity in Endometrial Cancer

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

The objectives for this study: 1. Investigate some of the causes for the racial disparity of endometrial cancer survival rates among black and white women 2. Examine the biologic correlates of aggressive behavior such as estrogen receptor status, p53 and HER-2/neu overexpression, and aromatase activity