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Evaluation of Treatment Response and Quality of Life of Esomeprazole for Reflux Esophagitis Patients

Evaluation of Treatment Response and Quality of Life of Esomeprazole for Reflux Esophagitis Patients - Evaluation of Treatment Response and Quality of Life of Esomeprazole for Reflux Esophagitis Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014449
Enrollment
80
Registered
2014-07-07
Start date
2013-09-27
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reflux Esophagitis

Interventions

esomeprazole 20mg/day for 8 weeks p.o.

Sponsors

Nagoya University Graduate School of Medicine, Department of Gastroentelorogy and Hepatology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient who is diagnosed as a reflux esophagitis and has been treated with PPI (expect for esomaprazole) for 4weeks, but GerdQ questionare shows insufficient therapeutic effect.

Exclusion criteria

Exclusion criteria: 1,Patients with a history of hypersensitivity to the study drug. 2,Patients in the administration of atazanavir sulfate or a Rirupibirin hydrochloride. 3,Patients with confirmed gastric ulcer, duodenal ulcer by endoscopy. 4,Patients who have unstable merger liver, kidney, heart disease or serious medical conditions. 5,History of gastrointestinal tract resection or vagotomy. 6,Pregnancy and lactation. 7,Patients treated with esomeprazole 14 days before obtaining informed consent 8,Patient in need of administration of the following agents other than the study drug during the study period (Excluding test drug), histamine H2-receptor antagonist, prokinetics, gastric mucosal protection, anticholinergic drugs, antacids, antidepressants, anti-anxiety drugs, steroids, bisphosphonates. 9,Patients who judged unsuitable for research participation.

Design outcomes

Primary

MeasureTime frame
Response rate by GerdQ questionnaire 4, 8 weeks after administration of esomeprazole

Secondary

MeasureTime frame
Influence of CYP2C19 Polymorphism on esomaplazole responsiveness

Countries

Japan

Contacts

Public ContactKohei Funasaka

Nagoya University Graduate School of Medicine Department of Gastroenterology and Hepatology

k-funa@med.nagoya-u.ac.jp052-744-2172

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026