Skip to content

Efficacy and safety of Intestinal bacteria capsule for the Treatment of Irritable Bowel Syndrome with small intestinal bacterial overgrowth

Efficacy and safety of Intestinal bacteria capsule for the Treatment of Irritable Bowel Syndrome with small intestinal bacterial overgrowth

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015142
Enrollment
Unknown
Registered
2018-03-10
Start date
2018-03-10
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Irritable Bowel Syndrome with small intestinal bacterial overgrowth

Interventions

Sponsors

Third Affiliated Hospital of Army Medical University (Field Surgery Institute)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Male or female, aged 16 to 75 years; 2) In accordance with irritable bowel syndrome diagnostic criteria of the Roman ?, patients are diagnosised Irritable Bowel Syndrome; 3) The patients were diagnosed small intestinal bacterial overgrowth; 4) No other serious disease, mental disorders, and have ability of normal communication; 5) Signed informed consent, agreed to participate in the study.

Exclusion criteria

Exclusion criteria: 1) complicated with other serious heart, liver, kidney, respiratory, digestive, blood, endocrine system disease; 2) abnormal liver meritorious service is significant or any of the following history of liver disease: 2 times higher than normal amount of AST and ALT limit, liver cirrhosis, hepatic encephalopathy history, history of history of esophageal varices or portal vein shunt; 3) a history of renal damage evidence or the following kidney disease: serum creatinine 1.5 times higher than normal limit; The history of dialysis; History or nephrotic syndrome; 4) the combination of various acute infection, tumor and severe arrhythmia, mental system disorders, drug or alcohol addiction; 5) pregnancy or lactation; 6) nearly four weeks with application of antibiotics, acid suppression, lactulose, probiotics, or other drugs affect gastrointestinal dynamic history; 7) it is difficult to finish with the visitor, or the various factors influencing the compliance.

Design outcomes

Primary

MeasureTime frame
SIBO eradication rate;IBS-SSS;

Secondary

MeasureTime frame
IBS-QOL;GSRS;16S rDNA;

Countries

China

Contacts

Public ContactChen Dongfeng

Third Affiliated Hospital of Army Medical University (Field Surgery Institute)

chendf1981@126.com+86 19923257387

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026