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Study on Clostridium Difficile Infection in Chinese Patients With Inflammatory Bowel Disease

Study on Prevalence, Risk Factors and Intestinal Microecology of Clostridium Difficile Infection in Chinese Patients With Inflammatory Bowel Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04179201
Enrollment
1000
Registered
2019-11-27
Start date
2017-09-13
Completion date
2020-09-30
Last updated
2019-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clostridium Infections, Inflammatory Bowel Diseases

Brief summary

In recent years, the incidence of Inflammatory Bowel Disease (IBD) has been increasing in China, which poses great challenges and burdens to the medical community due to its unknown etiology, recurrence and incurability. Co-infection is one of the important causes in IBD development. IBD accompanied with Clostridium Difficile Infection (CDI) can significantly decrease the treatment efficiency, leading to increased surgical rate, increased mortality, prolonged hospital stay, and increased hospital costs. Recently, several Chinese clinical guidelines about IBD or CDI have been published, but these guidelines are mainly based on the foreign studies. Compared with the developed countries, the lack of multi-center, large-scale and multi-test clinical trials and cohort studies caused limited understanding for IBD-CDI in China. Therefore, it is of great importance to carry out the multi-center clinical trials and analysis on IBD-CDI to improve the diagnostic and therapeutic efficiency in IBD-CDI patients Objective: 1. To evaluate the prevalence rate of IBD-CDI in Chinese adults in China based on the multi-center clinical trials.. 2. To analyze the related risk factors of IBD-CDI in China based on the multi-center clinical trials. 3. To analyze the intestinal flora of IBD-CDI patients via high-throughput sequencing.

Interventions

None listed

Sponsors

Xijing Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* 1.Inpatients with diagnostic criteria for ulcerative colitis and Crohn's disease in accordance with the consensus opinion on the diagnosis and treatment of inflammatory bowel disease in China in 2012 * 2.Willing to participate in the study; * 3\. Have the ability to understand and sign informed consent.

Exclusion criteria

* 1.Patients with infectious enteritis, intestinal tuberculosis, lymphoma, Behcet's disease or other intestinal diseases except inflammatory bowel disease; * 2.Pregnant or lactating women; * 3.Severe circulatory system, respiratory system, blood system, immune system, urinary system and other combined diseases or serious psychosomatic diseases.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence rate of IBD with CDI in Chinese adults3 yearsTo analyze the prevalence rate of IBD with CDI in Chinese adults based on the multicenter clinical trials.

Secondary

MeasureTime frameDescription
Risk factors of IBD with CDI in China3 yearsTo analyze the related risk factors of IBD with CDI in China based on the multicenter clinical trials. Including demographic data,severity of disease(Mayo score for ulcerative colitis and CDAI score for CD),laboratory results(ESR、CRP、WBC、Hb、RBC)and combination therapy.
Gut microbiota in patients with IBD-CDI,IBD and healthy volunteers by 16S rDNA sequencing3 yearsTo analyze the gut microbiota with IBD-CDI,IBD and healthy volunteers.Including fecal flora composition and the abundance analysis by 16S rDNA sequencing.

Other

MeasureTime frameDescription
Using PCR and ELISA to detect the positive rate of clostridium difficile in patients with IBD and healthy volunteers3 yearsTo compare the positive rate of clostridium difficile in patients with IBD and healthy volunteers by PCR and ELISA.

Countries

China

Contacts

Primary ContactYujie Zhang, MD
609183757@qq.com+8613891882872

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026