Viewing Study NCT05133193


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Ignite Modification Date: 2025-12-25 @ 1:11 AM
Study NCT ID: NCT05133193
Status: UNKNOWN
Last Update Posted: 2021-11-26
First Post: 2021-11-13
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Efficacy and Safety of 14-day Concomitant Therapy for Refractory Helicobacter Pylori Infection
Sponsor: Shandong University
Organization:

Study Overview

Official Title: Efficacy and Safety of 14-day Concomitant Therapy for Refractory Helicobacter Pylori Infection:A Pilot Study
Status: UNKNOWN
Status Verified Date: 2021-11
Last Known Status: NOT_YET_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: The purpose of this study is to evaluate efficacy of a 14-day concomitant therapy for the third-line treatment of Helicobacter pylori infection, and whether it is safe while maintaining an ideal eradication rates.
Detailed Description: Helicobacter pylori infects half of the world's population. H.pylori eradication is an effective approach to reduce the risk of developing gastric cancer. However, eradication rates of first-line therapy decreased over years due to the rapidly increasing antibiotic resistance of H. pylori worldwide. An ideal rescue therapeutic regimen to cure refractory H.pylori infection is currently warranted.

Few published paper evaluated the efficacy of 14-day furazolidone containing concomitant therapy in the third line treatment. This study aims to propose a new concomitant therapy for the patients with three or more treatment failure, and then evaluates whether adverse effects are tolerable. .

Study Oversight

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