Viewing Study NCT05002595



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Last Modification Date: 2024-10-26 @ 2:11 PM
Study NCT ID: NCT05002595
Status: COMPLETED
Last Update Posted: 2022-02-24
First Post: 2021-08-04

Brief Title: H Pylori Treatment Between Modified Quadruple Regimen and Tailored Therapy
Sponsor: Soonchunhyang University Hospital
Organization: Soonchunhyang University Hospital

Study Overview

Official Title: Comparison of Helicobacter Pylori Treatment Between Modified Quadruple Therapy and Tailored Eradication Based on the Presence of Clarithromycin Resistance
Status: COMPLETED
Status Verified Date: 2022-02
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 rate of H pylori resistance to antimicrobial agents including clarithromycin CAM has increased worldwide Eradication failure using triple therapy is strongly associated with CAM-resistant H pylori The tailored therapy is defined as a targeted H pylori eradication which emphasizes on predicting individual drug responses before treatment

Dual priming oligonucleotide DPO-based multiplex polymerase chain reaction PCR was developed to diagnose H pylori infection and identify CAM resistance The use of DPO-PCR has increased the tailored H pylori eradication rate in Korea If DPO-PCR testing is not available a 14-day modified bismuth-containing quadruple regimen is recommended as a first-line H pylori eradication However there is no comparison study between modified quadruple therapy and tailored eradication based on the presence of CAM resistance using DPO-PCR
Detailed Description: The investigators aim to evaluate the success rate adverse drug events and cost-effectiveness of modified quadruple therapy compared with tailored eradication based on the presence of CAM resistance

Study Oversight

Has Oversight DMC: None
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?: None