Viewing Study NCT02583659


Ignite Creation Date: 2025-12-24 @ 3:04 PM
Ignite Modification Date: 2026-02-24 @ 2:30 PM
Study NCT ID: NCT02583659
Status: UNKNOWN
Last Update Posted: 2015-11-11
First Post: 2015-10-19
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: The First-line Combined Chemotherapy for Advanced Gastric Cancer: A Prospective Observational Clinical Study
Sponsor: Huazhong University of Science and Technology
Organization:

Study Overview

Official Title: The First-line Combined Chemotherapy for Advanced Gastric Cancer: A Prospective Observational Clinical Study
Status: UNKNOWN
Status Verified Date: 2015-10
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This prospective cohort study aims to observe the efficacy and safety of the first-line combined chemotherapy for advanced gastric cancer(AGC) in Chinese population.
Detailed Description: 1. Establish a clinical database for the advanced gastric cancer patients treated with first-line combined chemotherapy in Tongji hospital.

1.1.Data including age, gender, smoking state, karnofsky performance score(KPS), disease history, clinical stage, primary tumor site, metastasis site, surgery, first-line chemotherapy, therapy after failure of first-line treatment, radiotherapy, toxicity, survival time, the time of free of progress, response were collected.

1.2.The peripheral blood samples were collected for further biomarker reserch.
2. Kaplan-Meier and Cox model will be used to analyze the overall survival(OS) and progression-free survival(PFS) of advanced gastric cancer.
3. Extract Deoxyribonucleic acid(DNA) from the the peripheral blood and research biomarkers related to the first-line combined chemotherapy for AGC.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: