Phase 1
N=31
Probiotic Use in Children Undergoing Hematopoietic Stem Cell Transplantation (HSCT)
Hematopoietic Organs; Disorder
Bottom Line
View on ClinicalTrials.gov: NCT01010867 ↗Enrolled (actual)
31
Serious AEs
0.0%
Results posted
Jul 2017
Primary outcome: Primary: Number of Lactobacillus Plantarum Bacteremia Infections — 0 Number of infections
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- Lactobacillus plantarum strains 299 and 299v (Drug)
- Age
- Pediatric · 2+ yrs
- Sex
- All
- Sponsor
- Columbia University
- Primary completion
- Oct 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Lactobacillus Plantarum Bacteremia Infections |
— | — |
| SECONDARY Adherence With the Prescribed Dose, Measured as the Percentage of Prescribed Probiotic Doses |
97 | — |
| SECONDARY Number of Non-lactobacillus Infections |
6 | — |
| SECONDARY Number of Acute Graft Versus Host Disease (GVHD) Events in HSCT Patients Who Have Been Administered Lactobacillus Plantarum |
9 | — |
Summary
Primary Objective:
1. To evaluate the safety of orally administered Lactobacillus plantarum strains 299 and 299v, a probiotic, in patients undergoing allogeneic myeloablative HSCT, as measured by incidence of Lactobacillus plantarum bacteremia.
Secondary Objectives:
1. To investigate the feasibility of administering Lactobacillus plantarum 299 and 299v to children and adolescents undergoing HSCT.
2. To describe the overall incidence of bacteremia in HSCT patients who have been administered Lactobacillus plantarum.
3. To describe the overall incidence of acute graft versus host disease (GVHD) in HSCT patients who have been administered Lactobacillus plantarum.
Eligibility Criteria
Inclusion Criteria
- All patients undergoing myeloablative allogeneic HSCT will be eligible. The source of stem cells can be from bone marrow, umbilical cord blood or cytokine mobilized peripheral blood. Donor can be human leukocyte antigen (HLA) matched sibling or parent, a related donor mismatched for a single HLA locus (class I or II), unrelated marrow or peripheral blood stem cell donor, or unrelated cord blood at least 4/6 antigen match (Class 1 or II).
- Patients of either gender and between 2 and 17.99 years of age
- Patients receiving any type of GVHD prophylaxis are eligible.
Exclusion Criteria
- Patients who have self-prescribed probiotics within 3 months of starting the conditioning regimen for stem cell transplant (consumption of yogurt products is allowed).
- Patients with known allergy to oats.
- Patients who have had any type of gut damage within the past three months; such as, previous bowel perforations; previous episode of Grade 4 neutropenic colitis or typhlitis.
- Patients with inflammatory bowel syndrome, short small bowel syndrome, Crohns Disease, Ulcerative Colitis, and patients with a history of bowel resections.
- Patients who have undergone a previous allogeneic HSCT.
Data sourced from ClinicalTrials.gov (NCT01010867). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.