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Pathophysiological Effects of Persistently Colonized Microbiome on Irritable Bowel Syndrome - Trial NCT06013410

Access comprehensive clinical trial information for NCT06013410 through Pure Global AI's free database. This phase not specified trial is sponsored by Second Affiliated Hospital, School of Medicine, Zhejiang University and is currently Recruiting. The study focuses on Irritable Bowel Syndrome. Target enrollment is 30 participants.

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NCT06013410
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diagnostic test
Trial Details
ClinicalTrials.gov โ€ข NCT06013410
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Pathophysiological Effects of Persistently Colonized Microbiome on Irritable Bowel Syndrome

Study Focus

Irritable Bowel Syndrome

colonoscopy

Interventional

diagnostic test

Sponsor & Location

Second Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, China

Timeline & Enrollment

N/A

Aug 25, 2023

May 15, 2026

30 participants

Primary Outcome

mirobiome difference of the fecal between IBS and health controls,mirobiome difference of the fecal between IBS and health controls,Metabolic changes between IBS and Healthy controls

Summary

The goal of this clinical trial is to explore the pathophysiological effects of the
 persistently colonized microbiome in irritable bowel syndrome (IBS) patients. The main
 questions it aims to answer are:
 
 Question 1: the microbiome difference of the biofilm between IBS and healthy patients.
 
 Question 2: the metabolic product patterns between IBS and healthy patients.
 
 Participants will need to take a colonoscopy examination, two gut mucosal biopsy samples will
 be collected during the examination.
 
 Researchers will compare the IBS and healthy control groups to see if there was the
 disease-specific pattern in the microbiome and metabolic product of the biofilm.

ICD-10 Classifications

Irritable bowel syndrome
Other and unspecified irritable bowel syndrome
Irritable bowel syndrome with mixed bowel habits [IBS-M]
Irritable bowel syndrome with predominant constipation [IBS-C]
Irritable bowel syndrome with predominant diarrhoea [IBS-D]

Data Source

ClinicalTrials.gov

NCT06013410

Non-Device Trial