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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