Trials / Not Yet Recruiting
Not Yet RecruitingNCT06437041
Effect of Antibiotic Pretreatment on the Efficacy of WMT in the Treatment of Irritable Bowel Syndrome
Effect of Antibiotic Pretreatment on the Efficacy of WMT in the Treatment of Irritable Bowel Syndrome in Adults: a Multi-center, Randomized, Placebo-controlledClinical Study
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 96 (estimated)
- Sponsor
- Faming Zhang · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a randomized controlled trial to explore the efficacy of antibiotic pretreatment on the efficacy of WMT in the treatment of Irritable bowel syndrome in adults: a multi-center, randomized, placebo-controlled clinical study
Detailed description
All included in the standard but do not accord with standard of any rule out subjects will be included in this study. Demographic characteristics, Gastrointestinal Symptoms Rating Scales(GSRS),IBS Symptom Severity Scaleand(IBS-SSS) 、Pittsburgh Sleep Quality Index(PSQI)、Self-rating Anxiety Scale(SAS)、Self-rating Depression Scale(SDS)and clinical outcomes will be collected. After the treatment, the efficacy and safety will be evaluated during the follow-up period.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ornidazole | Patients will receive three consecutive enemas of ornidazole 0.5g+50ml saline through the TET tube, followed by WMT treatment once daily for a duration of 3 days. |
| DRUG | Placebo | Patients will receive three consecutive enemas of placebo of equal volume through the TET tube, followed by WMT treatment once daily for a duration of 3 days |
Timeline
- Start date
- 2024-06-01
- Primary completion
- 2029-12-31
- Completion
- 2030-03-31
- First posted
- 2024-05-31
- Last updated
- 2024-05-31
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06437041. Inclusion in this directory is not an endorsement.