Enteroadsorbent Polymethylsiloxane vs Probiotic Lactobacillus Reuteri in the Treatment of Rotaviral Gastroenteritis
Primary Purpose
Rotavirus Gastroenteritis
Status
Completed
Phase
Phase 4
Locations
Croatia
Study Type
Interventional
Intervention
Polymethylsiloxane
Lactobacillus reuteri
Sponsored by
About this trial
This is an interventional treatment trial for Rotavirus Gastroenteritis
Eligibility Criteria
Inclusion Criteria:
- age 6-36 months
- proven rotavirus gastroenteritis
- symptom duration less than 48 hours
- informed consent of the parents/caregivers
Exclusion Criteria:
- rotavirus vaccination
- rotavirus infection in a patient's history
- severe acute or chronic illness with possible influence on rotavirus gastroenteritis outcome
Sites / Locations
- University Clinic for Infectious Diseases
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Polymethylsiloxane
Lactobacillus reuteri
Arm Description
Polymethylsiloxane (Enterosgel) is given 3 x 10 g for the initial two days, and 3 x 5 g for the next three days.
Probiotic Lactobacillus reuteri (BioGaia) is given 3 x 20 drops (which means 3 x 400,000.000 CFU) per day for five days.
Outcomes
Primary Outcome Measures
Gastroenteritis symptoms duration.
Duration of the loose stools, fever and vomiting.
Secondary Outcome Measures
Duration of the hospitalization of any kind.
Duration of the classic hospitalization or duration of daily hospital attending.
Total number of loose stools.
The total number of loose stools are measured.
Full Information
NCT ID
NCT04116307
First Posted
September 30, 2019
Last Updated
October 2, 2019
Sponsor
University Hospital for Infectious Diseases, Croatia
1. Study Identification
Unique Protocol Identification Number
NCT04116307
Brief Title
Enteroadsorbent Polymethylsiloxane vs Probiotic Lactobacillus Reuteri in the Treatment of Rotaviral Gastroenteritis
Official Title
Comparison of Clinical Efficacy of Enteroadsorbent Polymethylsiloxane vs Probiotic Lactobacillus Reuteri in the Treatment of Rotaviral Gastroenteritis in Infants and Toddlers.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2013 (Actual)
Primary Completion Date
May 31, 2017 (Actual)
Study Completion Date
May 31, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital for Infectious Diseases, Croatia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study evaluates a new drug, new enteroadsorbent polymethylsiloxane (Enterosgel) in the treatment of rotavirus gastroenteritis in children. Half of the participants received a new drug, polymethylsiloxane and half of the participants received standard treatment - probiotic L. reuteri (BioGaia).
Detailed Description
Polymethylsiloxane and probiotic L. reuteri both hasten symptoms of the rotavirus gastroenteritis but they do so by a different mode of action.
Polymethylsiloxane is an enteroadsorbent and it possibly acts by adsorption of viruses and doing so it prevents binding rotaviruses for enterocytes. Another mode of action can be forming a thin layer over the mucosal surfaces thus protects them from various damaging factors.
Probiotics help the healing of the intestinal mucosa presumably in few ways - by normalization of gut flora, by competition with pathogen bacteria for binding sites and nutrients and by stimulation of intestinal immune system.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotavirus Gastroenteritis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
130 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Polymethylsiloxane
Arm Type
Experimental
Arm Description
Polymethylsiloxane (Enterosgel) is given 3 x 10 g for the initial two days, and 3 x 5 g for the next three days.
Arm Title
Lactobacillus reuteri
Arm Type
Active Comparator
Arm Description
Probiotic Lactobacillus reuteri (BioGaia) is given 3 x 20 drops (which means 3 x 400,000.000 CFU) per day for five days.
Intervention Type
Dietary Supplement
Intervention Name(s)
Polymethylsiloxane
Other Intervention Name(s)
Enterosgel
Intervention Type
Dietary Supplement
Intervention Name(s)
Lactobacillus reuteri
Other Intervention Name(s)
BioGaia
Primary Outcome Measure Information:
Title
Gastroenteritis symptoms duration.
Description
Duration of the loose stools, fever and vomiting.
Time Frame
1-8 days.
Secondary Outcome Measure Information:
Title
Duration of the hospitalization of any kind.
Description
Duration of the classic hospitalization or duration of daily hospital attending.
Time Frame
30 days
Title
Total number of loose stools.
Description
The total number of loose stools are measured.
Time Frame
8 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
3 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
age 6-36 months
proven rotavirus gastroenteritis
symptom duration less than 48 hours
informed consent of the parents/caregivers
Exclusion Criteria:
rotavirus vaccination
rotavirus infection in a patient's history
severe acute or chronic illness with possible influence on rotavirus gastroenteritis outcome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Goran Tešović, MD, PhD
Organizational Affiliation
University Clinic for Infectious Diseases, Zagreb
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Clinic for Infectious Diseases
City
Zagreb
ZIP/Postal Code
10000
Country
Croatia
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Time Frame
The data are available for ten years.
Citations:
PubMed Identifier
33409259
Citation
Markovinovic L, Knezovic I, Kniewald T, Stemberger Maric L, Trkulja V, Tesovic G. Enteroadsorbent Polymethylsiloxane Polyhydrate vs. Probiotic Lactobacillus reuteri DSM 17938 in the Treatment of Rotaviral Gastroenteritis in Infants and Toddlers, a Randomized Controlled Trial. Front Pediatr. 2020 Dec 21;8:553960. doi: 10.3389/fped.2020.553960. eCollection 2020.
Results Reference
derived
Learn more about this trial
Enteroadsorbent Polymethylsiloxane vs Probiotic Lactobacillus Reuteri in the Treatment of Rotaviral Gastroenteritis
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