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Perioperative synbiotic treatment to prevent postoperative infectious complications after laparoscopic colorectal surgery

Phase 3
Conditions
Elective laparoscopic colorectal surgery
Registration Number
JPRN-UMIN000003439
Lead Sponsor
agoya Daini Red Cross Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
400
Inclusion Criteria

Not provided

Exclusion Criteria

In case significant changes are needed in the planning of surgery (e.g. addition of hepatectomy or urinary tract diversion). Those who prefer to drink beverages of synbiotics or those who dislike such products. Those who have difficulty in taking water because of the diseases, such as bowel obstruction. Those who cannot understand the concept of the study (e.g. dementia or mental disorders). Patients who do not have enough time to take synbiotics products for more than 7 days before surgery (e.g. when the surgery should be scheduled as soon as possible after the admission.)

Study & Design

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