Perioperative Gut Microbiota and Post-operative Ileus in Colorectal Cancer Patients
Data Collection
Collected from past medical records and data - RetrospectiveCase-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
Study start date: April 1, 2019
Actual date on which the first participant was enrolled.This study focuses on understanding postoperative ileus (POI), a common condition that can occur after abdominal surgery, particularly in patients with colorectal cancer. POI can cause symptoms such as abdominal swelling, nausea, vomiting, and difficulty passing stools, leading to extended hospital stays and increased risk of complications. The exact cause of POI is still unclear, but researchers believe that changes in gut bacteria during the surgery period may contribute to this condition. This study aims to explore how the gut microbiome of colorectal cancer patients changes during the time of surgery, and how these changes might be linked to POI. During the study, the composition of gut bacteria in colorectal cancer patients will be analyzed using advanced sequencing techniques. The study will compare changes in gut bacteria between two groups of patients. The primary outcomes of the study include understanding the diversity and structure of gut bacteria, as well as identifying specific types of bacteria that might be associated with POI. The study will also measure the time it takes for patients to have their first bowel movement after surgery, as this is an important indicator of gut recovery.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.40 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 35 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
First affiliated hospital of Harbin medical university
Harbin, ChinaOpen First affiliated hospital of Harbin medical university in Google Maps