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RECRUITING
NCT07792980
NA

AI-Assisted Microbiome Analysis for Evaluating the Efficacy of MPRO3 and Gut Environmental Changes in Colon Cancer Surgery Patients

Sponsor: hy Co., LTD.

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to evaluate the effects of MPRO3(probiotics mixture) supplementation on surgical outcomes and gut health in patients undergoing surgery for colon cancer.The main question is whether MPRO3 supplementation before and after surgery can reduce postoperative infectious complications compared with placebo.Participants will take either MPRO3 or a placebo once daily for 13 weeks, from 1 week before surgery to 12 weeks after surgery. Researchers will compare the two groups to assess postoperative infectious complications, other clinical outcomes, and changes in the gut microbiome.

Official title: AI-Assisted Microbiome Analysis for Evaluating the Efficacy of MPRO3 and Gut Environmental Changes in Colon Cancer Surgery Patients: A 13-Week, Randomized, Double-Blind, Placebo-Controlled Trial (AI-MPRO3 Study)

Key Details

Gender

All

Age Range

20 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-08-04

Completion Date

2028-04-12

Last Updated

2026-08-28

Healthy Volunteers

No

Conditions

Interventions

DIETARY_SUPPLEMENT

Placebo

Participants will receive one placebo capsule orally once daily after breakfast for 13 weeks.

DIETARY_SUPPLEMENT

MPRO3

Participants will receive one MPRO3 capsule orally once daily after breakfast for 13 weeks.

Locations (1)

Seoul ST. Mary's Hospital

Seoul, Seoul, South Korea