Skip to content

Methane and Hydrogen Breath Test for the Diagnosis of Small Intestinal Bacterial Overgrowth

Methane and Hydrogen Breath Test for the Diagnosis of Small Intestinal Bacterial Overgrowth

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06483360
Enrollment
750
Registered
2024-07-03
Start date
2024-09-01
Completion date
2025-12-31
Last updated
2024-08-27

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

Conditions

Small Intestinal Bacterial Overgrowth

Keywords

Small intestinal bacterial overgrowth, Methane and hydrogen breath test, Cut-off

Brief summary

To investigate whether the positive rates of methane and hydrogen breath test were different between the experimental group and the control group.

Detailed description

Small intestinal bacterial overgrowth (SIBO) refers to a syndrome of gastrointestinal symptoms caused by changes in the number and/or type of bacteria in the small intestine, and is considered to be secondary to changes in intestinal anatomy, slowing of intestinal motility, or abnormalities in gastrointestinal function. Clinical symptoms of SIBO are atypical, and are mainly characterized by bloating, belching, abdominal pain, diarrhea, constipation, and changes in stool shape, color, odor, and other characteristics. Since the clinical symptoms of SIBO are not specific and the clinical diagnosis criteria are not standardized, its treatment has not been given enough attention.

Interventions

None listed

Sponsors

First Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
West China Hospital
CollaboratorOTHER
First Affiliated Hospital of Kunming Medical University
CollaboratorOTHER
Second Affiliated Hospital, School of Medicine, Zhejiang University
CollaboratorOTHER
Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion criteria for the experimental group: 1. Age 18-65 years old and gender; 2. Patients with functional gastrointestinal disease are characterized by abdominal symptoms (abdominal distension, early satiety, diarrhea, constipation, abdominal pain, etc.) 3. have the autonomy to complete methane and hydrogen breath testing and gastrointestinal symptom scoring independently or with medical assistance; 4. able to complete the signing of informed consent as required. Inclusion criteria for the control group: 1. Age 18-65 years old and gender; 2. Healthy individuals without obvious typical gastrointestinal symptoms; 3. Autonomy to complete methane and hydrogen breath testing and gastrointestinal symptom scoring independently or with medical assistance; 4. Ability to complete the informed consent form as required.

Exclusion criteria

1. Patients whose gastroenteroscopy within one year indicated malignant tumor of digestive tract, or whose above examination proved peptic ulcer within two months; 2. A history of malignant tumors of the digestive system (not limited to the digestive tract), a history of inflammatory bowel disease, or a history of false or mechanical ileus; 3. Gastrointestinal resection, appendectomy and cholecystectomy within one year; 4. History of gastrointestinal perforation, gastrointestinal bleeding, cholangitis, acute and chronic pancreatitis within one year; 5. There is evidence of gastrointestinal tract infection (Helicobacter pylori, acute infectious enteritis); 6. History of type I diabetes and primary hypothyroidism; 7. Confirmed lactose malabsorption, lactose intolerance, and pancreatic exocrine insufficiency; 8. Within 4 weeks, a history of antibiotic administration; 9. Within 2 weeks, history of endoscopy; 10. Within 1 week, history of taking gastrointestinal stimulants, probiotics, laxatives; 11. 1 day prior to testing, eating fermentable foods (yogurt, kimchi, soy sauce, tempeh, oats, beer, etc.); 12. Not fasting 8 hours prior to testing; 13. Smoking, strenuous exercise 2 hours before and during the test; 14. Preparation for pregnancy, pregnancy, breastfeeding women, or overall poor compliance, or other conditions that the investigator believes need to be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Methane and hydrogen breath test results of experimental and control groupsJuly 1, 2024 to December 31, 2024To investigate whether the positive rates of methane and hydrogen breath test were different between the experimental group and the control group.

Contacts

Primary ContactJing-yuan Fang, MD,Ph.D
fangjingyuan_new@163.com13046678061

Outcome results

None listed

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