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Trial Title: A Novel Oral Synbiotic Formula in Reducing Adenoma Recurrence and Colorectal Neoplasia-related Bacterial Gene Markers

NCT ID: NCT05592886

Condition: Colorectal Neoplasms
Colorectal Adenoma
Colorectal Cancer

Conditions: Official terms:
Colorectal Neoplasms
Adenoma
Recurrence

Conditions: Keywords:
Adenoma recurrence
Bacterial marker

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Prevention

Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Intervention:

Intervention type: Other
Intervention name: SMT04 formula
Description: The SMT04 formula is a synbiotic containing probiotics and prebiotics
Arm group label: Intervention arm

Intervention type: Other
Intervention name: Active placebo
Description: The active placebo is 2 mg Vitamin C with an inert substance made of starch filler. The flavor, coloring and appearance are unidentifiable to the study product.
Arm group label: Placebo arm

Summary: This double blinded randomized controlled trial aims to assess the efficacy of a novel oral synbiotic formula (SMT04) in reducing adenoma recurrence and colorectal neoplasia-related bacterial gene markers after endoscopic resection of colorectal advanced neoplasia.

Detailed description: Recent evidence has demonstrated the association between altered gut microbiome environment and the progression of colorectal cancer (CRC) from its precancerous lesions. Some pathogenic species of bacteria, including Fusobacterium nucleatum, Escherichia Coli and Bacteroides fragilis, have shown to be significantly enriched in CRC patients. This gut dysbiosis process also brings with its diagnostic potential for recurrent adenomas. Previous study found a panel of bacterial gene markers, including "m3" from Lachnoclostridium, F. nucleatum (Fn), Bacteroides clarus (Bc) and Clostridium hathewayi (Ch) could be used in detecting adenoma recurrence after polypectomy in a retrospective study. In addition, these microbial biomarkers may have prognostic potential and provide an option as therapeutic target. Probiotics, including the genera Bifidobacterium and Lactobacillus, have shown to be able to inhibit tumorigenesis and progression of CRC in animal studies. Prebiotics are non-digestible dietary ingredients with protective effects against cancer by selectively stimulating the growth and activity of beneficial colonic microbiota. The combination of probiotics and prebiotics, known as synbiotic, may be more efficient in preventing CRC than either one alone. The investigators' unpublished data showed that the new probiotic formula containing Bifidobacterium strains has a negative correlation with CRC-related bacterial gene markers. Subjects treated with SMT04 showed significantly higher levels of the individual Bifidobacterium species at week 2 to week 5 compared with baseline levels. There was a significant decrease in the bacterial gene markers (Fn, m3 and 4Bac CRC risk score) from week 2 to week 12 compared with baseline levels in the SMT04 group but not in the control group. The synbiotic formula (SMT04) is the combination of probiotic formula and several heat-resistant prebiotics. It remains unclear that whether this synbiotic formula can produce a sustained effect in reduction of adenoma recurrence and colorectal neoplasia related bacterial gene markers in long-term.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - 1. Subjects have advanced colorectal neoplasia requiring endoscopic resection (endoscopic mucosal resection, endoscopic submucosal dissection, etc.); - They have received high quality colonoscopies before or during endoscopic resection (defined as a full colonoscopy with successful caecal intubation, and a Boston Bowel Preparation Scale ≧2 in each colonic segment); - Aged 18-90 years old; - Written informed consent obtained Exclusion Criteria: - Known residual colorectal neoplasia not removed (except hyperplastic polyps); - Contraindications to endoscopic resection due to deep submucosal invasion; - Prior surgical resection of colon; - Personal history of hereditary polyposis syndrome or inflammatory bowel disease; - Known pregnancy or lactation; - Immunocompromised status (e.g. on immunosuppressants (except 5-aminosalicylic acid or short term use of corticosteroids <4 weeks), on chemotherapy, bone marrow or solid organ transplant, human immunodeficiency virus, congenital immune deficiency); - Advanced comorbid conditions (defined as American Society of Anesthesiologists grade 4 or above); - Refusal to undergo surveillance colonoscopy.

Gender: All

Minimum age: 18 Years

Maximum age: 90 Years

Healthy volunteers: No

Locations:

Facility:
Name: Prince of Wales Hospital

Address:
City: Shatin
Country: Hong Kong

Status: Not yet recruiting

Contact:
Last name: Louis Lau

Facility:
Name: Prince of Wales Hospital

Address:
City: Hong Kong
Country: Hong Kong

Status: Recruiting

Contact:
Last name: Louis Lau

Start date: December 15, 2022

Completion date: December 31, 2025

Lead sponsor:
Agency: Chinese University of Hong Kong
Agency class: Other

Source: Chinese University of Hong Kong

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05592886

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