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Clinical Trials/KCT0008756
KCT0008756
Not yet recruiting
未知

Efficacy evaluation of digestive in patients who underwent gastrectomy for gastric cancer

ational Cancer Center0 sites240 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
ational Cancer Center
Enrollment
240
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
ational Cancer Center

Eligibility Criteria

Inclusion Criteria

  • •1\. Patients 19 years of age or older
  • •2\. Patients who underwent gastrectomy for gastric cancer
  • •3\. Patients who do not need adjuvant chemotherapy and under follow\- up
  • •4\. Patient having no abnormal finding in endoscopic examination at 3 months (±4 weeks), postoperatively
  • •5\. Patients having postprandial satiety or early satiety for more than 3 days per week at 3 months (±4 weeks) after surgery (postprandial distress syndrome of ROMA IV classification, postprandial distress syndrome

Exclusion Criteria

  • •1\. Vulnerable subjects (pregnant patients, those lacking communication ability, etc.)
  • •2\. Patients who have taken drugs classified as digestive agents within 7 days from the time of registration
  • •3\. Patients taking drugs that affect digestive function an evaluation (anti\-cancer drugs, adrenal cortical hormone drugs, anti\-inflammatory drugs, etc.)
  • •4\. Patients with genetic problems of galactose intolerance
  • •5\. Patients judged unsuitable for participation in this study by the researcher

Outcomes

Primary Outcomes

Not specified

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