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Analysis of the improvement effect of the abdominal symptom by the proton pump inhibitor for patients recieved chemotherapy

Not Applicable
Conditions
Colon cancer patients received chemotherapy
Registration Number
JPRN-UMIN000003077
Lead Sponsor
Department of Gastroenterology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

1)Patients with peptic ulcers 2)Patients with severe GERD 3)Patients who has past history of allergy for the drugs used in this study 4)Patients with severe heart disease, liver disease,or renal disease 5)Pregnant females 6)Lacting woman 7)Patients who has past history of allergy for the drugs used in this study 4)Patients who has coexisting severe disease 5)Patient whom examination doctor judged improper as testee

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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