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Modulation of intestinal microecology by rifaximin in patients with irritable bowel syndrome - a single-center, prospective, open-label clinical study

Modulation of intestinal microecology by rifaximin in patients with irritable bowel syndrome - a single-center, prospective, open-label clinical study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082111
Enrollment
Unknown
Registered
2024-03-21
Start date
2024-03-30
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

irritable bowel syndrome

Interventions

treatment grouop:oral administration of rifaximin
control group:None (samples from subjects before treatment)

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Individuals who meet all the following criteria can be included in this study 1) Diagnosed with IBS-D according to the Rome IV criteria, with a degree of abdominal pain = 3 (moderate or severe symptoms interfering with normal activity); 2) Aged between the 18 and 65 years old, regardless of gender; 3) Suitable for the treatment; 4) Voluntary acceptance of the treatment and signing an informed consent form in accordance with the relevant provisions of GCP.

Exclusion criteria

Exclusion criteria: Individuals with any of the following cannot be included in this study 1) With general or specific contraindications to the provided medication; 2) Combined with cardiovascular, cerebrovascular, hepatic, renal, hematopoietic system, hyperthyroidism, diabetes mellitus, inflammatory bowel disease and other serious primary diseases diseases, or serious diseases affecting their survival (such as tumors, etc.) and psychiatric patients. 3) Women who are pregnant, breastfeeding, or planning to be pregnant. 4) Are suspected or have a history of alcohol or drug abuse. 5) Cognitive impairment that prevents full informed consent. 6) Patients who have received medication for IBS within the last 2 weeks and who have participated in other clinical trials within the last month. 7) Patients with conditions unsuitable for inclusion in the study assessed by the researchers.

Design outcomes

Primary

MeasureTime frame
fecal metagenome;fecal metabolome;

Secondary

MeasureTime frame
Irritable Bowel Syndrome-Symptom Severity Scale;Irritable Bowel Syndrome-Quality of Life;

Countries

China

Contacts

Public ContactXiaohua Hou

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

houxh@hust.edu.cn+86 130 3514 3646

Outcome results

None listed

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