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Study to Investigate the Treatment Benefits of Probiotic Streptococcus Salivarius K12 for Hospitalised Patients (Non-ICU) With COVID-19

Primary Purpose

Covid19

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Standard of care
BLIS K12
Sponsored by
King Edward Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years (both sexes)
  • Hospitalized confirmed (RT-PCR) COVID-19 patients (not already in ICU) admitted for treatment of COVID-19 and not receiving mechanical ventilatory support
  • Patients who have signed informed consent

Exclusion Criteria:

  • Patients with proven hypersensitivity or allergic reaction to the tested formula
  • Patients who decline to participate in the study

Sites / Locations

  • King Edward Medical University Teaching Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard of care

BLIS K12

Arm Description

In this arm patients will receive the standard COVID-19 care as per the hospital guidelines.

In this arm patients will receive the BLIS K12 as add-on to the standard COVID-19 care

Outcomes

Primary Outcome Measures

Recovery and live discharge
Number of patients with clinical improvement

Secondary Outcome Measures

Hospitalisation days
The effect of K12 treatment in reducing the hospitalisation days
Effect on inflammatory markers
Numbers of patients with improvement in the inflammatory markers
ICU transfer
Reduction in the rate of ICU transfer

Full Information

First Posted
September 11, 2021
Last Updated
January 22, 2022
Sponsor
King Edward Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT05043376
Brief Title
Study to Investigate the Treatment Benefits of Probiotic Streptococcus Salivarius K12 for Hospitalised Patients (Non-ICU) With COVID-19
Official Title
Study to Investigate the Treatment Effect of Probiotic Streptococcus Salivarius K12 in Hospitalised Patients (Non-ICU) With COVID-19
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
September 10, 2021 (Actual)
Primary Completion Date
November 21, 2021 (Actual)
Study Completion Date
November 21, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
King Edward Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomised, open-label and controlled clinical trial aimed to investigate the adjuvant treatment benefits of probiotic Streptococcus salivarius K12 in hospitalised mild-to-moderate patients with COVID-19 disease.
Detailed Description
Boosting the immunity and maintaining a healthy and balanced microflora at oropharyngeal environment of people through probiotics supplementation has been proposed as a possible strategy to protect human host from respiratory tract infections. A slow-dissolved oropharyngeal probiotic formula containing S. salivarius K12 has been clinically demonstrated to improve the upper respiratory tract microbiota protecting the host from pathogenic bacteria, fungi, and viruses, thereby reducing the incidence of viral respiratory tract infections and bacterial co-infections. S. salivarius K12 has been proposed as a promising agent for prophylactic or probiotic treatments to protect individuals during the outbreak of seasonal or emerging respiratory infection diseases. S. salivarius K12 strain, commonly known as BLIS K12, is a highly safe, and extensively-studied probiotic that resides in the oral cavity. BLIS K12 has a solid scienctific rationale for helping to prevent streptococcal pharyngitis and/or tonsillitis, ear infections (otitis media) and to help treat halitosis. It is a specific strain of Streptococcus Salivarius, which secretes powerful anti-microbial molecule called Bacteriocin-Like-Inhibitory Substances (BLIS). The ingredient is believed to support healthy bacteria in the mouth for long-term fresh breath and immune support. It is proposed that the oral administration of the strain K12 to hospitalized COVID-19 patients (not already in ICU) receiving supplementary oxygen (not invasive oxygen theraphy) to exploit the "ventilation" and helping S. salivarius (K12) to move from the mouth (it is an oral colonizer) to the lungs, colonizing them. The idea is that the lung presence of K12 could strategically reduce the lung and immune capability to release pro-inflammatory cytokines, thus preventing excessive lung inflammation, and the need to proceed to ICU and death.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of care
Arm Type
Active Comparator
Arm Description
In this arm patients will receive the standard COVID-19 care as per the hospital guidelines.
Arm Title
BLIS K12
Arm Type
Experimental
Arm Description
In this arm patients will receive the BLIS K12 as add-on to the standard COVID-19 care
Intervention Type
Drug
Intervention Name(s)
Standard of care
Intervention Description
Standard COVID-19 care as per the hospital guidelines
Intervention Type
Dietary Supplement
Intervention Name(s)
BLIS K12
Intervention Description
Daily 2 oral BLIS K12 tablets for up to 14 days.
Primary Outcome Measure Information:
Title
Recovery and live discharge
Description
Number of patients with clinical improvement
Time Frame
From day 1 to day 14
Secondary Outcome Measure Information:
Title
Hospitalisation days
Description
The effect of K12 treatment in reducing the hospitalisation days
Time Frame
From day 1 to day 14
Title
Effect on inflammatory markers
Description
Numbers of patients with improvement in the inflammatory markers
Time Frame
From day 1 to day 14
Title
ICU transfer
Description
Reduction in the rate of ICU transfer
Time Frame
From day 1 to day 14

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years (both sexes) Hospitalized confirmed (RT-PCR) COVID-19 patients (not already in ICU) admitted for treatment of COVID-19 and not receiving mechanical ventilatory support Patients who have signed informed consent Exclusion Criteria: Patients with proven hypersensitivity or allergic reaction to the tested formula Patients who decline to participate in the study
Facility Information:
Facility Name
King Edward Medical University Teaching Hospital
City
Lahore
State/Province
Punjab
ZIP/Postal Code
54000
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Study to Investigate the Treatment Benefits of Probiotic Streptococcus Salivarius K12 for Hospitalised Patients (Non-ICU) With COVID-19

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