Viewing Study NCT02523404


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Study NCT ID: NCT02523404
Status: COMPLETED
Last Update Posted: 2016-08-29
First Post: 2015-08-12
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA)for Lung Cancer
Sponsor: Fuda Cancer Hospital, Guangzhou
Organization:

Study Overview

Official Title: HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA) for Lung Cancer: Clinical Trial
Status: COMPLETED
Status Verified Date: 2015-10
Last Known Status: None
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: The purpose of this study is to evaluate the safety and efficacy of HepaSphere interventional therapy using digital subtraction angiography(DSA)for lung cancer.
Detailed Description: By enrolling patients with lung cancer adapted to enrolled criteria, this study will document for the first time the safety and the short and long term efficacy of HepaSphere interventional therapy using digital subtraction angiography(DSA)for lung cancer.

Study Oversight

Has Oversight DMC: True
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?: