Viewing Study NCT05191888



Ignite Creation Date: 2024-05-06 @ 5:07 PM
Last Modification Date: 2024-10-26 @ 2:22 PM
Study NCT ID: NCT05191888
Status: RECRUITING
Last Update Posted: 2022-01-14
First Post: 2021-12-28

Brief Title: 14-day PCAB-based High-dose Dual Therapy and14-day PCAB-based Triple Therapy vs 14-day PPI-based Reverse Hybrid Therapy
Sponsor: Kaohsiung Medical University
Organization: Kaohsiung Medical University

Study Overview

Official Title: 14-day PCAB-based and Reverse Hybrid Therapy Fro Helicobacter Pylori
Status: RECRUITING
Status Verified Date: 2022-01
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: 1 Test for Helicobacter pylori The test items include urease test histology bacterial culture serology and urea breath test At least two positive results can be used to confirm the diagnosis
2 To ensure that the research results are not artificially distorted this trial is a randomized study Random allocation which means that the subjects will use the random number table generated by a computer similar to the lottery to determine the treatment group accept one of the following schemes 111
Detailed Description: Helicobacter pylori Hpylori infect more than 50 of humans globally This study were 1 to test whether the efficacies of 14-day PCAB-based high-dose dual therapy and 14-day PPI-based reverse hybrid therapy can achieve a higher eradication rate than 14-day PCAB-based triple therapy in the first-line treatment of H pylori infection 2 to compare the eradication rates of 14-day PCAB-based and PPI-based bismuth quadruple therapies in the second-line treatment of H pylori infection and 3 to examine the impacts of antibiotic resistance of H pylori as well as CYP3A4 CYP2C19 and IL-1B -511 genotypes of host on the eradication efficacies of anti-H pylori treatments

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