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NCT03099876

A Study on Eradication Rate of Triple Therapy According to Treatment Period and CYP2C19 Polymorphisms in H.Pylori Patients

Status unknown Last updated 7 April 2017
What this trial tests

trial testing treatment period in Helicobacter Pylori Infection in 320 participants. Status unknown.

Timeline
1 March 2017
Primary endpoint
1 December 2017
1 December 2018

Quick facts

Lead sponsorIl-Yang Pharm. Co., Ltd.
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment320
Start date1 March 2017
Primary completion1 December 2017
Estimated completion1 December 2018
Sites4 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Il-Yang Pharm. Co., Ltd. — full company profile →

Who can join

Adults 20 to 80, any sex, with Helicobacter Pylori Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study compared efficacy and safety of basic triple therapy according to treatment period. This study evaluated Effect of CYP2C19 genetic polymorphisms on the efficacy

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The prolongation effect of ilaprazole-based standard triple therapy for Helicobacter pylori.
    Lee SW, Moon SJ, Kim SH, Jung SH, et al · · 2020 · cited 4× · PMID 32957336 · DOI 10.1097/md.0000000000022137

Verify or expand the search:

Other recruiting trials for Helicobacter Pylori Infection

Currently open trials in the same condition.

Other Il-Yang Pharm. Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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