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

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT05592886
Collaborator
(none)
246
2
2
36.5
123
3.4

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: SMT04 formula
  • Other: Active placebo
N/A

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The investigators' unpublished data showed that the new probiotic formula containing Bifidobacterium strains has a negative correlation with CRC-related bacterial gene markers.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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
246 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
A Double Blinded Randomized Controlled Trial of a Novel Oral Synbiotic Formula in Reducing Adenoma Recurrence and Colorectal Neoplasia-related Bacterial Gene Markers
Actual Study Start Date :
Dec 15, 2022
Anticipated Primary Completion Date :
Dec 15, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention arm

Receive SMT04 formula

Other: SMT04 formula
The SMT04 formula is a synbiotic containing probiotics and prebiotics

Placebo Comparator: Placebo arm

Receive active placebo

Other: Active placebo
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.

Outcome Measures

Primary Outcome Measures

  1. The incidence of metachronous recurrent colorectal adenoma at year 1 (local or at other sites) [1 year]

    The proportion of patients with metachronous recurrent adenoma at year 1

Secondary Outcome Measures

  1. Incidence of recurrent colorectal advanced adenomas at year 1 [1 year]

    The proportion of patients with metachronous recurrent advanced adenoma at year 1

  2. Number of recurrent adenomas at year 1 [1 year]

    The number of recurrent colorectal adenoma per patient both in intervention and placebo arm

  3. Number of recurrent advanced adenomas at year 1 [1 year]

    The number of recurrent colorectal advanced adenoma per patient both in intervention and placebo arm

  4. Changes in the levels of bacterial gene markers [1 year]

    The change in the level of four bacterial gene markers tested by qPCR

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Prince of Wales Hospital Shatin New Territories Hong Kong
2 Prince of Wales Hospital Hong Kong Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Louis Lau, Prince of Wales Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Louis Ho Shing Lau, Clinical Assistant Professor, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05592886
Other Study ID Numbers:
  • 2022.360
First Posted:
Oct 25, 2022
Last Update Posted:
Dec 30, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Louis Ho Shing Lau, Clinical Assistant Professor, Chinese University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 30, 2022