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Effects of Chemotherapy clinical trials

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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: 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: NCT02087475 Recruiting - Surgery Clinical Trials

Perioperative FOLFIRI VS Adjuvant FOLFIRI in Resectable Advanced CRC Failed to Oxaliplatin

Start date: January 2011
Phase: Phase 3
Study type: Interventional

Colorectal cancer (CRC) is one of the most leading causes of cancer death in China. Although multiple treatment modalities including surgery, radiotherapy and chemotherapy have been developed, the prognosis of advanced CRC still remains poor. While around 30% of resectable advanced CRC could be cured. This study is designed to compare perioperative FOLFIRI versus adjuvant FOLFIRI in resectable advanced CRC who exposed to oxaliplatin in open-label, phase III mode.

NCT ID: NCT01915134 Recruiting - Clinical trials for Effects of Chemotherapy

Endostatin in Combination With Chemotherapy for Metastatic Nasopharyngeal Carcinoma

Start date: August 2013
Phase: Phase 3
Study type: Interventional

The investigators designed this study to evaluate the efficiency and the acute toxicities of recombinant human endostatin (endostar) combined with chemotherapy in the metastatic nasopharyngeal carcinoma (NPC).

NCT ID: NCT01749072 Recruiting - Clinical trials for Non-small Cell Lung Cancer

Vinorelbine-ifosfamide Versus Gefitinib for EGFR Gene Mutation Negative Non-small Cell Lung Cancer Patients

Start date: December 2012
Phase: Phase 2
Study type: Interventional

In the National Comprehensive Cancer Network (NCCN) guideline for NSCLC, epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) is recommended as the third-line treatment for EGFR gene mutation negative NSCLC patients who failed to the first-line platinum doublet chemotherapy [i.e. paclitaxel-carboplatin (PC) or gemcitabine-cisplatin (GP)] and the second-line chemotherapy with docetaxel or pemetrexed. But as we know, if patients had no EGFR gene mutation, EGFR-TKI treatment is not effective. The overall survival is short and the objective response rate is low. As for EGFR gene wild type patients with good performance status, besides EGFR-TKI treatment, other first generation cytotoxic drugs i.e. vinorelbine or ifosfamide maybe an alternative treatment. So the purpose of this clinical trial is to compare the effectiveness and safety of vinorelbine-ifosfamide with gefitinib in advanced or metastatic EGFR gene mutation negative NSCLC patients.