PROACRE: Evaluation of the Impact of an Amoxicillin and Amoxicillin/Clavulanic Acid Resistant Probiotic on Key Clinical Outcomes in Children Treated With Amoxicillin or Amoxicillin/Clavulanic Acid

Sponsor
Liaquat University of Medical & Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05840588
Collaborator
(none)
300
1
2
8.7
34.5

Study Details

Study Description

Brief Summary

Amoxicillin or Amoxicillin/Clavulanic acid antibiotic therapy has been shown to be associated with disrupting the microbiota population particularly Bifidobacterium, which may have further GI clinical implications.

The present randomized clinical trial is aimed to assess if probiotic Bifidobacterium breve PRL2020 can help modulate the Bifidobacterium population and its clinical implications after antibiotic Amoxicillin or Amoxicillin/Clavulanic acid antibiotic therapy.

Condition or Disease Intervention/Treatment Phase
  • Drug: Antibiotic Treatment
  • Dietary Supplement: Probiotic Bifidobacterium breve PRL2020 treatment
N/A

Detailed Description

Treatment with Amoxicillin or Amoxicillin/Clavulanic acid is one of the most common antibiotic therapies used against various infections both in children and adults. These antibiotics can create an imbalance in the intestinal microbiota, altering its structure with a reduction in bacterial richness and, more specifically, in the abundance of bifidobacteria. This opened the window for further evaluations of the effect of this antibiotic combination on the composition of gut microbiota. The alteration can lead to intestinal symptoms such as pain, bloating, abdominal distension, flatulence, diarrhea, and constipation. In study by L. Mancabelli et al. (2021), Bifidobacterium breve PRL2020 has shown greatest resistance to Amoxicillin and Amoxicillin/Clavulanic acid. Currently available scientific data, however, have not yet analyzed the ability of B. breve PRL2020 to counteract the reduction of bifidobacteria that may occur in the human gut during the antibiotic therapy with Amoxicillin or Amoxicillin/Clavulanic acid, and neither its ability to avoid the consequent clinical relapse.

The purpose of this randomized, controlled, prospective, single-center, non-profit study will be to evaluate the efficacy and safety of the administration of Bifidobacterium breve PRL2020 in pediatric patients (> 4 years of age), treated with the antibiotic Amoxicillin or Amoxicillin/Clavulanic acid, in the improvement of the symptoms due to the pharmacological treatment and in the contrast of the fall of the Bifidobacterium cluster.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluation of the Impact of an Amoxicillin and Amoxicillin/Clavulanic Acid Resistant Probiotic on Key Clinical Outcomes in Children Treated With Amoxicillin or Amoxicillin/Clavulanic Acid
Actual Study Start Date :
Apr 10, 2023
Anticipated Primary Completion Date :
Oct 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Probiotic Bifidobacterium breve PRL2020

Patients in this arm will receive Probiotic Bifidobacterium breve PRL2020 (20 billion CFU) 2 sticks/day for 10 days in addition to the antibiotic Amoxicillin or Amoxicillin/Clavulanic acid.

Drug: Antibiotic Treatment
Antibiotic Amoxicillin or Amoxicillin/Clavulanic acid

Dietary Supplement: Probiotic Bifidobacterium breve PRL2020 treatment
Probiotic Bifidobacterium breve PRL2020

Active Comparator: Control

Patients in this arm will receive only antibiotic Amoxicillin or Amoxicillin/Clavulanic acid.

Drug: Antibiotic Treatment
Antibiotic Amoxicillin or Amoxicillin/Clavulanic acid

Outcome Measures

Primary Outcome Measures

  1. Incidence of any Gastrointestinal upset [3 weeks]

    Safety or tolerability of the treatments in both groups

Secondary Outcome Measures

  1. Probiotic colonization rate [3 weeks]

    Assessment of the probiotic colonization rate in both groups particularly effect on Bifidobacterium cluster

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children aged between 4-12 years, of either gender, with a bacterial infection and the use of antibiotic therapy with Amoxicillin or Amoxicillin/clavulanic acid under a Physician's prescription.

  • Informed written consent from legal guardian

Exclusion Criteria:
  • Use of antibiotics within 3 months prior to enrolment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Liaquat University Hospital Jamshoro Pakistan

Sponsors and Collaborators

  • Liaquat University of Medical & Health Sciences

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dr. Amjad Khan, Professor, Liaquat University of Medical & Health Sciences
ClinicalTrials.gov Identifier:
NCT05840588
Other Study ID Numbers:
  • LUMHS/REC/180
First Posted:
May 3, 2023
Last Update Posted:
May 3, 2023
Last Verified:
Apr 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
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 3, 2023