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NCT07144475CompletedPhase 4

Comparison of Probiotic Effects on the Outcomes of Patients After Colorectal Cancer Surgery

Comparison of Probiotic Effects of Lactobacillus Casei Shirota With Lactobacillus Acidophilus on the Outcomes of Patients After Colorectal Cancer Surgery: A Study of Gastrointestinal Function, Sepsis Incidence, C-Reactive Protein, Interleukin 6 and Length of Stay

Source: ClinicalTrials.gov · Last updated 27 Aug 2025

Brief summary (registry, in English)

This clinical trial aims to compare the effects of administering Lactobacillus casei Shirota probiotics with Lactobacillus acidophilus on the outcomes of patients after colorectal cancer surgery. Researchers will compare probiotic to see if Lactobacillus casei Shirota improves gastrointestinal function, sepsis incidence, C-reactive protein (CRP), interleukin 6 (IL-6), and length of stay better than Lactobacillus acidophilus. Participants will take probiotics three times daily for three days before surgery.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
90 (actual)
First submitted
18 Aug 2025
Start date
1 Jan 2024
Primary completion date
30 Nov 2024
Lead sponsor
Dharmais National Cancer Center Hospital
NCT number
NCT07144475

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 90
  • From 1 Jan 2024 to the primary completion date, 30 Nov 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with chronic diseases such as HIV, uncontrolled diabetes mellitus (, uncontrolled cardiovascular disease and kidney failure
  • Patients with a history of regular probiotics, or steroids, or antibiotics consumption
  • Patients with anatomical disorders of the gastrointestinal system
  • Patients with immunocompromised conditions.

Other

  • The patient or patient's family refused to be included in the study

Who the study is looking for

  • 1\. Patients who were diagnosed with colorectal cancer and would undergo resection surgery at Dharmais Cancer Hospital

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Medicine, University of Indonesia
Coordinator of this site? Confirm its status
JakartaIndonesiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.