Effect of Carbon Dioxide Insufflation and Appendix on the Restoration of Intestinal Microecology After Colonoscopy.

December 6, 2022 updated by: Zhongshan Hospital Xiamen University

Study on the Influencing Factors of Intestinal Microecology Changes Before and After Colonoscopy

The goal of this observational study is to learn about Influencing factors of intestinal microecological changes before and after colonoscopy. The main questions it aims to answer are:

  • [question 1] The process of colonoscopic gas insufflation affects the intestinal microecology. Will the use of carbon dioxide gas insufflation can reduce the changes of intestinal microecology after colonoscopy?
  • [question 2] Can the appendix act as a reservoir for microorganisms to accelerate the recovery of intestinal microecology after colonoscopy?

Participants will be asked to accept colonoscopy for once. Group 1(Control group) will be insufflated air during the colonoscopy; Group 2(Carbon dioxide group) will be insufflated carbon dioxide during the colonoscopy; Group 3(After appendectomy group) will be insufflated air during the colonoscopy.

Since Group 1 is comparison group, the investigators will compare Group 2 to see if carbon dioxide gas insufflation can reduce the changes of intestinal microecology after colonoscopy. Meanwhile, compare Group 3 to see if the appendix can accelerate the recovery of intestinal microecology after colonoscopy.

Study Overview

Detailed Description

Usually, gastroenteroscopy requires gas insufflation to expand the lumen to facilitate endoscopic insertion and detailed observation of the mucosa. In the past, the use of air as an insufflation gas in endoscopic operations was simple and inexpensive, but because its main component was nitrogen, it was difficult to be absorbed by the gastrointestinal mucosa. Therefore, the endoscopist often needs to fully aspirate the gas when the procedure is completed. However, studies have shown that about 50% of patients still complain of abdominal pain after colonoscopy, and 12% of patients still have severe abdominal pain even after 24 hours. In contrast, carbon dioxide (CO2) has been used in endoscopy of the digestive tract in recent years because it can be rapidly absorbed by the gastrointestinal mucosa, and has attracted the attention of endoscopists.

The gastrointestinal mucosa absorbs CO2 at a rate 160 times faster than nitrogen. Because of this property, many people consider replacing air in endoscopic operations. Its potential value was first demonstrated in animal tests: the recovery time of intestinal lumen dilation and increased intraluminal pressure was significantly shortened after intestinal lumen injection of CO2 in rats. Meta-analysis showed no significant difference in safety, gas volume, or cecal intubation rate between the two groups for CO2 insufflation during colonoscopy, but less postoperative abdominal pain, abdominal distention, and less postoperative gastrointestinal exhaust in the CO2 group. The low postoperative pain score and low increase in abdominal circumference may be due to the rapid absorption of CO2 by the gastrointestinal mucosa, suggesting that residual gas after colonoscopy is the main cause of abdominal pain. CO2 is a non-flammable gas that is safe for electroresection and has been widely used in laparoscopic surgery. For patients with chronic obstructive pulmonary disease (COPD) who require endoscopy, it is worth exploring whether the use of CO2 in endoscopy causes CO2 retention. In one study of 77 endoscopic participants with obstructive ventilation dysfunction and 308 endoscopic participants without concomitant obstructive ventilation dysfunction, there was no difference in end-tidal volume CO2 between the two groups, and the peak tidal volume CO2 peak was less than 60 mmHg in both groups, suggesting that endoscopic use of CO2 is still safe for people with concomitant obstructive ventilation dysfunction.

The current study has found that the intestinal preparation of the colonoscopy, as well as the colonoscopy operation itself, has a certain impact on the intestinal microbiome, although this effect can be partially recovered over a period of time, but the current study has found that this change may also be permanent, but whether it will cause long-term metabolic, immune or clinical changes in the host is unknown. Compared with conventional air injection, CO2 may change less about the hypoxic environment of the intestine, thereby reducing the impact on the normal intestinal microbiome.

Based on this hypothesis, the investigators will conduct randomized, controlled experiments to investigate the effects of conventional air and CO2 insufflation on the intestinal microbiome and metabolites.

In addition, some studies have called the appendix a "reservoir" of gut microbes. First, the mucosal flora of the appendix is similar to the rest of the colon; Secondly, the fecal microbiota composition of mice changed after appendectomy. The appendix preserves a small amount of intestinal bacteria as "seeds", once the intestinal flora is imbalanced, the "seed bank" will be used for cultivation, when the appendix is removed, it is equivalent to the "seed bank" is destroyed, so once the intestinal flora is imbalanced, there may be a delay in the recovery of the intestinal microecology.

Based on this hypothesis, the investigators will conduct controlled experiments to compare the intestinal microbiome recovery after colonoscopy in healthy people and people after appendectomy, and explore the impact of appendix on intestinal microbiome recovery.

This study was a single-center study, and 20 cases were initially included in the control group, CO2 group and after appendectomy group.

Study Type

Observational

Enrollment (Actual)

38

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Fujian
      • Xiamen, Fujian, China, 361001
        • Zhongshan Hospital Xiamen University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

The patients in the after appendectomy group were patients who underwent appendectomy in the Department of General Surgery, Zhongshan Hospital Xiamen University within 3 years.

The other volunteers are residents of Xiamen City.

Description

Inclusion Criteria:

  • Age 18-40 years old, gender is not limited, no underlying diseases;
  • BMI between 18.5-23.9 kg/m2;
  • Fecal Bristol score type III-IV in the past week;
  • No history of alcohol consumption or alcohol consumption equivalent to ethanol should not exceed 140g per week for men and 70g per week for women.
  • Add a criterion to after appendectomy group:Patients who underwent appendectomy in the Department of General Surgery of Zhongshan Hospital Xiamen University within 3 years.

Exclusion Criteria:

  • Those who use antibiotics, antifungal drugs, antiviral drugs, probiotics, prebiotics, synbiotics and drugs that may affect the intestinal microecology within 1 month;
  • Those who have acute enteritis or chronic enteritis and other diagnosed chronic bowel diseases in the past 1 month;
  • Those who have digestive symptoms such as blood in the stool, constipation, bloating, abdominal pain, diarrhea and so on in the past 1 month
  • History of digestive surgery (including gastrointestinal polyp resection, gastrointestinal tumor surgery and diversion surgery, etc.).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Control group
Healthy people were randomly divided into CO2 group and control group, with 20 cases in each group. After bowel preparation, volunteers underwent colonoscopy, with air routinely insufflated into the control group during colonoscopy.
Carbon dioxide group
Healthy people were randomly divided into CO2 group and control group, with 20 cases in each group. After bowel preparation, volunteers underwent colonoscopy, with CO2 insufflated into the control group during colonoscopy.
Carbon dioxide is insufflated to dilate the bowel lumen during colonoscopy.Record the amount of gas insufflated during colonoscopy.
After appendectomy group
Volunteers after appendectomy were included in the appendectomy group. After bowel preparation, all volunteers underwent colonoscopy, air routinely insufflated into the appendectomy group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The intestinal microbiota composition
Time Frame: Before bowel cleansing, after colonoscopy, 7、14 and 28 days after the treatment
Changes in the intestinal microbiome are observed by detecting the feces at the specific time point.Then, factors affecting the recovery of the intestinal microbiome are assessed based on their changes.
Before bowel cleansing, after colonoscopy, 7、14 and 28 days after the treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hongzhi Xu, Zhongshan Hospital Xiamen University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2022

Primary Completion (Actual)

July 14, 2022

Study Completion (Anticipated)

December 31, 2022

Study Registration Dates

First Submitted

November 24, 2022

First Submitted That Met QC Criteria

November 24, 2022

First Posted (Actual)

December 5, 2022

Study Record Updates

Last Update Posted (Estimate)

December 9, 2022

Last Update Submitted That Met QC Criteria

December 6, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2022-014

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

All IPD that underlie results in a publication.

IPD Sharing Time Frame

Starting 6 months after publication.

IPD Sharing Access Criteria

To the public.

IPD Sharing Supporting Information Type

  • Study Protocol
  • Informed Consent Form (ICF)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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