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Stomach Neoplasms clinical trials

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NCT ID: NCT00352833 Completed - Gastric Cancer Clinical Trials

Safety and Efficacy Study With Catumaxomab in Patients After Curative Resection of a Gastric Adenocarcinoma

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

Investigation of the outcome of an adjuvant treatment with catumaxomab as compared to surgery alone in patients after curative resection of a gastric adenocarcinoma in order to gain more detailed information primary on safety, tolerability and feasibility and secondary on relevant efficacy parameters.

NCT ID: NCT00343239 Completed - Stomach Neoplasms Clinical Trials

Docetaxel in Locally Advanced Gastric Adenocarcinoma

NEOTAX
Start date: June 2006
Phase: Phase 2
Study type: Interventional

Study objectives: To determine Ro resection rate of Docetaxel, cisplatin and fluorouracil combination for the treatment of neoadjuvant gastric carcinoma.

NCT ID: NCT00342004 Completed - Breast Cancer Clinical Trials

A Prospective Cohort Study of Occupational Exposures and Cancer Risk Among Women

Start date: May 1, 1997
Phase:
Study type: Observational

A prospective cohort study is proposed to evaluate occupational and environmental risk factors for cancer among women in Shanghai, China. Approximately 75,000 women aged 40-69 who reside in eight geographically defined communities in two urban districts of Shanghai will be recruited via a community-based cancer education program. All eligible subjects will be invited by local health workers from the neighborhood health station to the clinic for an interview and selected anthropometric measurements. The interview will elicit information on demographic background, diet, lifestyle factors, medical history, lifetime occupational history and residential history for the past 20 years. In addition, the women will be asked for information on their husbands' current and usual occupations, and demographic and a few other exposure factors. A spot urine sample and 10 ml of blood will be collected from all cohort members and stored at -70 degrees C for future assays of urine metabolites and DNA and hemoglobin adducts of selected occupational and environmental carcinogens, and polymorphic genes encoding enzymes that are involved in metabolism of relevant carcinogens. Cohort members and their husbands will be followed for cancer outcomes through biennial recontact and linkage with files of the population-based Shanghai Cancer Registry, of the Shanghai Vital Statistics, and of the Shanghai Resident Registry. Medical records and pathology slides will be reviewed for all cancer cases to verify their diagnosis. Post-diagnostic blood samples will be obtained from all cohort members diagnosed with cancer during the follow-up period and stored for future methodologic and etiologic studies. The proposed initial study period is 5 years, with an average follow-up of about 3.5 years. We anticipate, however, that follow-up will continue for 10 years or more.

NCT ID: NCT00323830 Completed - Gastric Cancer Clinical Trials

Phase III Randomized Trial of Adjuvant XP Chemotherapy and XP/RT for Resected Gastric Adenocarcinoma

Start date: October 2004
Phase: Phase 3
Study type: Interventional

The objective of the trial is to compare disease-free survival between adjuvant capecitabine/cisplatin alone vs capecitabine/cisplatin with radiotherapy (chemoradiation) in curatively resected gastric cancer patients.

NCT ID: NCT00320515 Completed - Neoplasm, Gastric Clinical Trials

Study of Pemetrexed Plus Cisplatin in Advanced Gastric Cancer

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

This is a multicenter, single arm, open-label Phase 1/2 study of pemetrexed plus cisplatin for patients with unresectable, advanced gastric cancer who had no prior palliative chemotherapy. Phase 1 was designed to determine the optimal dose of pemetrexed for its phase 2, which has been completed and now a total of 60 qualified patients will be enrolled in the phase 2 of this study. The treating physician will determined the maximum number of cycles of pemetrexed plus cisplatin that a patient may receive in this study.

NCT ID: NCT00313872 Completed - Gastric Cancer Clinical Trials

Phase III Trial of DP Followed by FOLFIRI or the Reverse Sequence in Unresectable Gastric Cancer

Start date: May 2003
Phase: Phase 3
Study type: Interventional

To assess the optimal sequence of the palliative chemotherapy regimen (DP --> FOLFIRI vs FOLFIRI --> DP) in metastatic gastric cancer patients.

NCT ID: NCT00313599 Completed - Breast Cancer Clinical Trials

Lapatinib and Paclitaxel in Treating Patients With Advanced Solid Tumors

Start date: February 2006
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Lapatinib may help paclitaxel work better by making tumor cells more sensitive to the drug. Lapatinib may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving lapatinib together with paclitaxel may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of lapatinib when given together with paclitaxel in treating patients with advanced solid tumors.

NCT ID: NCT00310115 Completed - Lung Cancer Clinical Trials

Motivational Counseling in Preventing Smoking Relapse After Pregnancy in Pregnant Women Who Quit Smoking During Pregnancy

Start date: April 2002
Phase: N/A
Study type: Observational

RATIONALE: Motivational counseling may help prevent pregnant women from smoking again after pregnancy. PURPOSE: This randomized clinical trial is studying three different types of counseling to see how well they work in preventing smoking relapse after pregnancy in pregnant women who quit smoking during pregnancy.

NCT ID: NCT00296335 Completed - Stomach Cancer Clinical Trials

Trial of Adjuvant Chemotherapy for Gastric Cancer

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

This is a phase III randomized study designed to evaluate the efficacy of mitomycin, doxifluridine, and cisplatin compared to mitomycin and doxifluridine.

NCT ID: NCT00296322 Completed - Stomach Cancer Clinical Trials

Trial of Adjuvant Chemotherapy for Gastric Cancer

Start date: October 2001
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate the efficacy of the intraperitoneal chemotherapy with early mitomycin administration and adding cisplatin to prolonged treatment with doxifluridine compared to mitomycin plus doxifluridine in resected advanced gastric cancer.