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Phase II study to evaluate the Synbiotics efficacy on reducing the incidence of postoperative infectious complications after liver resection.

Phase II study to evaluate the Synbiotics efficacy on reducing the incidence of postoperative infectious complications after liver resection. - SYNERGI Study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031240051
Enrollment
254
Registered
2024-04-25
Start date
2024-07-05
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with primary biliary tract cancer without distant metastases(with/without tissue diagnosis)

Interventions

Control group: One packet each of probiotic placebo and prebiotic placebo (two packets in total) three times a day daily during the following periods: From 14 days before hepatectomy to the day befor
Prebiotics,Probiotics,Synbiotics

Sponsors

Sawada Yu
Lead Sponsor
Endo Itaru
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients aged between 20 and 80 years at the time of enrolment. 2) Patients diagnosed with primary biliary tract cancer without distant metastasis. 3) Patients with a general health status (ECOG PS) of 0-1. 4) Patients with no previous treatment for biliary tract cancer prior to enrolment. 5) Patients scheduled for hepatic resection beyond the hepatic lobectomy with biliary reconstruction. 6) Patients who give written free and voluntary consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1) Patients who have taken other probiotics, synbiotic products and other antiflatulent, including supplements, in the seven days prior to obtaining consent, and who have are unable to discontinue taking other probiotics, synbiotic products and other antiflatulent, including supplements, from the date of obtaining consent until the end of the postoperative infectious complication assessment. 2) Patients who are unable to consume the study products 3) Patients who have already participated or will participate during the study period in other clinical trials or clinical studies 4) Patients who are judged to be unsuitable as subjects by the principal investigator or research assistant.

Design outcomes

Primary

MeasureTime frame
Incidence of post-operative infectious complications

Secondary

MeasureTime frame
Surgical mortality, Number of days on antimicrobials, Number of postoperative hospital days, Incidence of pre-operative cholangitis, Detection of bacteria in blood, Intestinal microbiota, Intestinal organic acid concentration ,Detection of bacteria in tumor tissue, Detection of bacteria in bile, Detection of bacteria in drainage fluid, Incidence of liver failure

Contacts

Public ContactYu Sawada

Yokohama City University Hospital

t116036e@yokohama-cu.ac.jp+81-45-787-2650

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026