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Randomized controlled trials for the efficacy between famotidine alone and combination of famotidine and egualen sodium hydrate on gastric ulcer healing for following eradication therapy for Helicobactor pylori

Not Applicable
Conditions
Gastric ulcer for following eradication therapy for Helicobactor pylori
Registration Number
JPRN-UMIN000007010
Lead Sponsor
Tokai University School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients with drug allegy 2.Patient taking Atananavir sulfate,Pimozide and Ergatamine-containing drugs 3.Patient who has been mononucleosis 4.Patients with severe liver and renal dysfunction, and serious heart-lung complication. 5.Pregnant, females who suckles, or females who wish to become pregnant 6.Patients who have eradication therapy of Helicobactor pylori infection 7.Patient who take PPI or H2RA within 1 month before obtaining informed consent 8.Patients who take mucosal protective medicine within 2 weeks before obtaining informed consent 9.Others,patients who are judged to be inadequate to participate in this trial by the investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The healing rate of gastric ulcer within 8 weeks
Secondary Outcome Measures
NameTimeMethod
The healing rate of gastric ulcer after 8 weeks QOL score (GSRS) after 2 weeks and 8 weeks
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