sefulness of postoperative probiotics in patients who underwent right hemicolectomy for colon cancer

Not Applicable

Recruiting

• Conditions: Neoplasms

• Registration Number: KCT0005392
• Lead Sponsor: The Catholic University of Korea, Uijeongbu St. Mary’s Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 12 July 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

? Adult men and women aged 20 to 80 years old
? Patients with colorectal cancer diagnosed histologically and imagingly, and who are scheduled for right colon resection
? Before the clinical trial begins, consent to participation in this clinical trial and sign a written consent.

Exclusion Criteria

? Those suffering from metastatic colon cancer
? Those who received chemotherapy or radiation therapy before surgery
? Patients with a history of severe cerebrovascular disease (cerebral infarction, cerebral hemorrhage, etc.), severe heart disease (unsafe angina, myocardial infarction, arrhythmia requiring heart failure treatment)
? Those with neurological or psychologically important medical history or currently suffering from a disease
? Those with a history of alcoholism or substance abuse
? People with immune system, infectious, gastrointestinal diseases (inflammatory bowel disease)
? Uncontrolled thyroid disease
? Creatinine is more than twice the normal upper limit of the test
? Those whose AST(GOT) and ALT(GPT) are more than 3 times the normal range
? Patients with uncontrolled hypertension (160/100mmHg or more, measured after 10 minutes of rest for the subject)
? Patients with uncontrolled diabetes (fasting blood sugar greater than 180mg/dl)
? Those who have taken or used probiotics or antibiotics within the last 1 week
? Pregnant women, lactating women, women of childbearing age who have a pregnancy plan or who do not agree with the selection of appropriate contraceptive methods
? Patients who have not performed the planned operation (right colon resection)
? Those who are judged to be inappropriate for this clinical trial

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluation of bowel movements using the number of bowel movements per day and Bristol stool chart

Secondary Outcome Measures

Name	Time	Method
Cancer patient quality of life questionnaire (EORTC QLQ-C30)