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Effects of Chemotherapy clinical trials

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NCT ID: NCT02454647 Completed - Gastric Cancer Clinical Trials

Induction Chemotherapy, Chemoradiotherapy and Surgery in Locally Advanced Gastric Cancer Patients

Start date: September 2013
Phase: N/A
Study type: Observational

The aim of this study is to evaluate the efficacy of a neoadjuvant approach in patients with locally advanced gastric cancer and the identification of prognostic factors.

NCT ID: NCT02423278 Recruiting - Gastric Cancer Clinical Trials

The Long-term Effect of D4 Lymphadenectomy for Gastric Cancer

Start date: January 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The main purpose of this study is to evaluate the effect of extensive lymphadenectomy procedure in treatment of gastric cancer. This study is designed as a open-label, multi-centers, randomized controlled trial. The overall survival and free disease survival are primary outcomes, with postoperative complication, hospital charges, and life quality as secondary outcomes.

NCT ID: NCT02395341 Completed - Clinical trials for Effects of Chemotherapy

The Longitudinal Ovarian Reserve Study

Start date: May 2007
Phase: N/A
Study type: Observational

Postmenarchal female cancer patients scheduled to undergo cancer therapy may enroll in this study to assess changes in existing and novel surrogate measures of fertility potential before, during and after chemotherapy. Measures of fertility potential to be tested include ultrasound imaging for antral follicle counts and ovarian volumes, endocrine evaluation, and assessment of oxidative stress.

NCT ID: NCT02375776 Completed - Prostate Cancer Clinical Trials

Improving Outcomes in Cancer Patients on Oral Anti-Cancer Medications Using a Multi-modal Mobile Health Intervention

CORA
Start date: March 2015
Phase: N/A
Study type: Interventional

This study evaluates a smart phone based mobile application designed for patients with Renal Cell and Prostate Cancer taking oral anti-cancer medications. (OAMs) All participants will be patients at the Dana Farber Cancer Institute in Boston, Massachusetts. Half of the participants will use the mobile application for a 3 month period along with their usual care. Half of the participants will just receive usual care. The investigators hope to show that cancer patients taking OAMs who use the mobile application will be better connected to their care team and will develop increased competency for self-care which will primarily increase medication adherence.

NCT ID: NCT02324595 Completed - Clinical trials for Peritoneal Cavity Cancer

Minimally Invasive Interval Debulking Surgery in Ovarian Neoplasm: a Feasibility Study

MISSION
Start date: December 2013
Phase: Phase 2
Study type: Interventional

Phase II multicentric study

NCT ID: NCT02306837 Recruiting - Clinical trials for Effects of Chemotherapy

Consolidation Chemotherapy After Autologous Stem Cell Transplantation for Lymphoid Malignancies

Start date: September 2014
Phase: Phase 2
Study type: Interventional

To imporve the outcome of patients with relapsed/refractory lymphoma, we conduct a clinical trial to test the efficacy and feasibility of consolidation chemotherapy after autologous stem cell transplantation

NCT ID: NCT02226380 Recruiting - Gastric Cancer Clinical Trials

FOLFOX6 as Neoadjuvant Chemotherapy in Local Advanced Gastric Cancer

FOLFOX6
Start date: October 2013
Phase: Phase 2
Study type: Interventional

Purpose: This aim of the study is to evaluate the efficacy and safety of neoadjuvant chemotherapy with the modified FOLFOX6(mFOLFOX6) regimen and its impact on survival on a series in local advanced gastric cancer patients. Patients and methods: The study is a prospective non-randomized study. Patients with histopathologically confirmed and locally advanced gastric cancer(T2-T4 or N+) are enrolled in the study. Patients are given mFOLFOX6 scheme for 3 cycles.A radical gastrectomy and a D2 lymphadenectomy was will be scheduled 3-6 weeks after the completion of the preoperative chemotherapy. Down-staging is assessed comparing pretreatment clinical staging with postoperative pathologic staging on patients who underwent radical surgery. Tumor down-staging and the grade of pathologic response are included in a statistical correlation between tumor regression induced by mFOLFOX6 neoadjuvant chemotherapy and survival.The primary endpoint is 3-year overall survival, secondary endpoints are disease-free survival, R0 resection rate, toxicity and prediction of response.

NCT ID: NCT02169388 Recruiting - Colorectal Cancer Clinical Trials

Intestinal Microflora in Colorectal Cancer (CRC) After Chemotherapy

Start date: June 2014
Phase: Phase 1
Study type: Interventional

Probiotics modulate the gut microflora and immune status in CRC,which can reduce the side effects of chemotherapy such as diarrhea,infection,neutropenia etc.

NCT ID: NCT02121405 Suspended - Surgery Clinical Trials

Randomized Trial of Primary Surgery Followed Selective Radiochemotherapy for Rectal Cancer With MRI Negative CRM

PSSR
Start date: October 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether primary radiotherapy can be omitted for the locally advanced rectal cancer with Magnetic Resonance Imaging (MRI) negative circumferential margin.

NCT ID: NCT02116231 Not yet recruiting - Clinical trials for Effects of Chemotherapy

The Role of Adding Concurrent Chemotherapy to IMRT in the Treatment of Stage II Nasopharyngeal Carcinoma

Start date: April 2014
Phase: Phase 2
Study type: Interventional

The study is designed to compare Intensity Modulated Radiotherapy (IMRT) in combination with concurrent chemotherapy and IMRT alone in treatment of stage II nasopharyngeal carcinoma.