Effect of Probiotics on Immunosuppressive-drug-associated Diarrhea Among Renal Transplant Recipients

Sponsor
State University of New York - Upstate Medical University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06150287
Collaborator
(none)
70
2
23

Study Details

Study Description

Brief Summary

The goal of this pilot project is to 1) examine whether oral administration of probiotics are helpful in reducing immunosuppressive drugs-associated diarrhea and adhering to the required dose of immunosuppressive drugs and 2) determine how this treatment works by examining fecal microbiome and immunological markers among living and deceased donor renal transplant recipients. The main questions it aims to answer are:

  1. Does low dose probiotics effective in reducing immunosuppressive drugs-associated diarrhea?

  2. Does probiotics effective in reducing inflammation?

  3. Is there any connection between fecal microbiome and immunological markers?

Participants will receive one probiotics capsule or placebo capsule daily for 6 months from the onset of diarrhea post-surgically. Researchers will compare the data obtained through probiotics group and placebo group to answer the above mentioned research questions.

Condition or Disease Intervention/Treatment Phase
  • Other: Florajen Digestion
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomized, double-blinded, placebo-controlled, single-center pilot/exploratory trialrandomized, double-blinded, placebo-controlled, single-center pilot/exploratory trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Effect of Probiotics on Immunosuppressive-drug-associated Diarrhea Among Renal Transplant Recipients
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
May 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Probiotics Group

Participants will receive one probiotics capsule immediately after the onset of post-surgical non-infectious diarrhea. Depending on the onset of diarrhea, the timeline for this study is 6 months.

Other: Florajen Digestion
Florajen Digestion is a probiotics. One probiotics capsule contains 15 billion Colony Forming Unit (CFU) of live microorganisms. No live microorganisms are present in the placebo capsules.
Other Names:
  • Placebo
  • Placebo Comparator: Placebo Group

    Participants will receive one placebo capsule immediately after the onset of post-surgical non-infectious diarrhea. Depending on the onset of diarrhea, the timeline for this study is 6 months.

    Other: Florajen Digestion
    Florajen Digestion is a probiotics. One probiotics capsule contains 15 billion Colony Forming Unit (CFU) of live microorganisms. No live microorganisms are present in the placebo capsules.
    Other Names:
  • Placebo
  • Outcome Measures

    Primary Outcome Measures

    1. Reduction in immunosuppressive drugs-associated diarrhea [GI questionnaire and Bristol Stool Chart will be collected daily for six months from the onset of post-surgical, non-infectious diarrhea.]

      Gastrointestinal (GI) questionnaire and Bristol Stool Chart will be used to measure this outcome through Chi-Square test.

    2. Analysis of inflammatory biomarkers [Whole blood will be collected three times for six months: baseline (on the day of transplant), 3 month and six month from the onset of post-surgical, non-infectious diarrhea. three and six months]

      Inflammatory biomarkers including TNF (tumor necrosis factor) superfamily proteins, IFN (interferon) family proteins, Treg cytokines and matrix metalloproteinases (MMP) [processed through Bio-Rad's Multiplex System) will be analyzed through general linear model analysis of variance (GLM ANOVA).

    3. Association between inflammatory markers and fecal microbiome [Stool samples will be collected seven times for six months: baseline (on the day of transplant), then monthly once from the onset of post-surgical, non-infectious diarrhea.]

      Fecal microbial DNA will be analyzed through 16S PCR followed by Next-Gen sequencing. Pearson correlation analysis will be performed.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Received living or deceased donor kidney, subjects will be monitored peri-operatively

    • Presence of mild to severe diarrhea (> 3X loose stools/day); include type 6 and 7 in the Bristol Stool Chart.

    • Has been on adjusted and/or maintenance dose of calcineurin inhibitors, antimetabolites and steroid regimen. Treatment of rejection including administration of steroids, intravenous immunoglobulin/plasmapheresis, rituximab and anti- thymocytes are also acceptable in this research.

    Exclusion Criteria:
    • Pregnant and lactating women

    • Has been receiving probiotics treatment

    • Recurrence of gastrointestinal diseases including inflammatory bowel diseases, diverticulosis, irritable bowel syndrome. Had past surgical history of gastric bypass.

    • Diagnosed with cancer

    • Presence of infectious diarrhea, fever and high WBC count. Infectious diarrhea is defined by PCR negative for community acquired diarrhea panel [positive for Sapo virus, Noro virus, Clostridium difficile (positive for toxin A and B), Yersinia eneterocolitica [(positivefor toxin A and B) and enteropathogenic E. coli (positive Shiga toxins)].

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • State University of New York - Upstate Medical University

    Investigators

    • Principal Investigator: Reza Saidi, State University of New York - Upstate Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    State University of New York - Upstate Medical University
    ClinicalTrials.gov Identifier:
    NCT06150287
    Other Study ID Numbers:
    • 2044457
    First Posted:
    Nov 29, 2023
    Last Update Posted:
    Nov 29, 2023
    Last Verified:
    Oct 1, 2023
    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
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by State University of New York - Upstate Medical University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 29, 2023