Skip to content

Clostridium Butyricum CBM588® vs. Rifaximin for Symptomatic Uncomplicated Diverticular Disease (SUDD): A Real-World Retrospective Study

Management of Symptomatic Uncomplicated Diverticular Disease (SUDD) of the Colon With Clostridium Butyricum CBM588® Versus Rifaximin: Results From a Real-World Retrospective Italian Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06852274
Enrollment
70
Registered
2025-02-28
Start date
2023-03-01
Completion date
2024-10-31
Last updated
2025-05-18

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

Conditions

Diverticular Diseases, Gastro-Intestinal Disorder

Brief summary

This retrospective, real-world, single-center clinical study aimed to evaluate the effectiveness of probiotic Clostridium butyricum CBM588® (Butirrisan®) versus Rifaximin in the management of Symptomatic Uncomplicated Diverticular Disease (SUDD). Patients with diverticulosis and a history of mild-to-moderate diverticulitis were included, and their clinical outcomes were assessed using existing patient records. The study compared two treatment groups: Experimental Group: Clostridium butyricum CBM588® (Butirrisan®) + fiber supplementation. Control Group: Rifaximin + fiber supplementation. The primary endpoint was the reduction in SUDD symptoms, evaluated using patient-reported outcomes. Secondary outcomes included assessment of safety, risk of surgery, and changes in abdominal pain frequency and severity.

Detailed description

Diverticulosis is a common condition affecting up to 60% of individuals over 60 years old, with 10-25% developing Symptomatic Uncomplicated Diverticular Disease (SUDD). This condition is characterized by chronic low-grade inflammation, altered gut microbiota, and persistent abdominal symptoms such as bloating, pain, and irregular bowel habits. Traditional treatment often involves cyclic rifaximin therapy. However, recent studies have highlighted the potential of microbiome-modulating therapies, including probiotics such as Clostridium butyricum CBM588®, to improve gut health, reduce inflammation, and manage SUDD symptoms. This retrospective, real-world study reviewed clinical records of 70 patients who received treatment for SUDD at a single center. The data were extracted from routine clinical practice records, without any prospective patient recruitment. Patients were categorized into two groups: The probiotic group received Clostridium butyricum CBM588® (Butirrisan®) with fiber supplementation. The control group received Rifaximin 400 mg twice daily for 7-10 days per month, alongside fiber supplementation. Outcomes were measured based on symptom relief over a 12-month period, including the frequency and severity of abdominal pain, the risk of surgery, and patient-reported outcomes. The study provided real-world evidence on the potential benefits of Clostridium butyricum CBM588® in supporting a microbiome-targeted approach for managing SUDD, potentially reducing reliance on antibiotics and improving patient quality of life.

Interventions

DIETARY_SUPPLEMENTClostridium butyricum CBM588® (Butirrisan®)

Probiotic

DRUGRifaximin 400 mg Oral Tablet

Antibiotic

Sponsors

San Giovanni Addolorata Hospital
CollaboratorOTHER
Dr. Amjad Khan
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

This retrospective, real-world clinical study reviewed patient records to evaluate the effectiveness of Rifaximin with fiber supplementation for managing Symptomatic Uncomplicated Diverticular Disease (SUDD). Patients who received this antibiotic and fiber combination in a routine clinical setting were included. The study assessed symptom reduction, prevention of surgery, and changes in patient-reported outcomes. No prospective randomization was performed, and all data were derived from existing clinical records, reflecting routine clinical practice.

Intervention model description

This retrospective, real-world clinical study reviewed patient records to evaluate the effectiveness of Clostridium butyricum CBM588® (Butirrisan®) with fiber supplementation for managing Symptomatic Uncomplicated Diverticular Disease (SUDD). Patients who received this probiotic and fiber combination in a routine clinical setting were included. The study assessed symptom reduction, prevention of surgery, and changes in patient-reported outcomes. No prospective randomization was performed, and all data were derived from existing clinical records, reflecting routine clinical practice.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged ≥18 years * Diagnosed diverticulosis (confirmed by colonoscopy or CT scan) * History of mild-to-moderate diverticulitis * Symptomatic Uncomplicated Diverticular Disease (SUDD) requiring management

Exclusion criteria

* Prior abdominal surgery * History of inflammatory bowel disease (IBD) or colorectal cancer * Use of antibiotics or probiotics within 4 weeks prior to study entry * Severe chronic comorbidities (e.g., advanced liver or kidney disease) * Pregnancy or breastfeeding * Patients with acute diverticulitis within the past 3 months

Design outcomes

Primary

MeasureTime frameDescription
Change in Symptoms of Diverticular Disease12 monthsAssessment Tool: Patient-reported outcome questionnaires derived from clinical records. Description: Evaluation of symptom relief, including changes in abdominal pain, bloating, and bowel habit irregularities, based on patient records.

Secondary

MeasureTime frameDescription
Assessment of Safety and Tolerability of Clostridium butyricum CBM588®12 monthsReview of adverse events and overall tolerability of probiotic therapy as documented in clinical records.
Incidence of Surgical Intervention in Patients with Diverticular Disease12 monthsPercentage of patients requiring surgical intervention due to complications of diverticular disease, as confirmed by medical records. Measurement Tool: Review of surgical records and patient medical charts. Unit of Measure: % of patients requiring surgery.
Changes in Abdominal Pain Frequency, Duration, and Severity12 monthsSymptom tracking via a validated pain scale extracted from patient records. Frequency Scale: 1: \<1x/week, 2: 1-2x/week, 3: 3-6x/week, 4: Daily. Duration Scale: 1: \<30 min, 2: 0.5-1h, 3: 1-6h, 4: \>6h. Severity Scale: 0: No pain, 1: Mild, 2: Moderate, 3: Severe, 4: Very severe.

Countries

Italy

Outcome results

None listed

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