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Beta-glucans for Hospitalised Patients With COVID-19

Primary Purpose

COVID-19

Status
Not yet recruiting
Phase
Phase 2
Locations
Chile
Study Type
Interventional
Intervention
MC 3x3
Placebo
Sponsored by
Wohlstand Pharmaceutical
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 focused on measuring beta-Glucans, Therapy, Signs and Symptoms, Mechanical ventilation, Inflammation, Survival

Eligibility Criteria

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

Inclusion Criteria:

  • Adult participants with an infection caused by SARS-CoV-2 confirmed with a reverse-transcription polymerase chain reaction (RT-PCR) obtained from a nasopharyngeal swab.

Exclusion Criteria:

  • Life expectancy < 6 months
  • Currently receiving invasive mechanical ventilation at baseline.
  • Cognitive impairment that precludes the use of WURSS or understanding the informed consent form.
  • Refusal to participate.

Sites / Locations

  • Hospital Gustavo Fricke

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Beta-Glucans

Placebo

Arm Description

Patients allocated to this arm will receive MC 3x3, an oral supplement containing 25mg of 1,3 beta-Glucans daily for up to three consecutive days.

Participants allocated to this arm will receive a placebo that will be identical in form to the MC 3x3 pills used the interventional arm. These doses will be scheduled daily and administered orally for up to three consecutive days.

Outcomes

Primary Outcome Measures

Symptom severity
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Symptom severity
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Symptom severity
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Symptom severity
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Symptom severity
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Symptom duration
Total time with disease manifestations attributable to COVID-19.
Clinical recovery
Number of patients without clinical complaints attributable to COVID-19

Secondary Outcome Measures

C-Reactive protein levels
C-Reactive protein levels measured at various time intervals during the hospitalisation.
Absolute lymphocyte count
Absolute lymphocyte counts measured at various time intervals during the hospitalisation.
Neutrophil to lymphocyte ratio
Neutrophil to lymphocyte ratios measured at various time intervals during the hospitalisation.
Intensive Care Unit Admission
Proportion of patients requiring admission to an intensive care unit in each study group
Invasive mechanical ventilation
Proportion of patients requiring invasive mechanical ventilation in each study group
Survival
Proportion of patients that survived COVID-19 in each study group
Hospital Stay
Total stay within the hospital amongst participants

Full Information

First Posted
July 15, 2022
Last Updated
December 9, 2022
Sponsor
Wohlstand Pharmaceutical
Collaborators
Concentra Educación e Investigación Biomédica
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1. Study Identification

Unique Protocol Identification Number
NCT05465798
Brief Title
Beta-glucans for Hospitalised Patients With COVID-19
Official Title
Beta-glucans as Immune Modulators Amongst Hospitalised Patients With COVID-19: A Pilot Randomised Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2023 (Anticipated)
Primary Completion Date
October 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wohlstand Pharmaceutical
Collaborators
Concentra Educación e Investigación Biomédica

4. Oversight

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

5. Study Description

Brief Summary
This randomised trial aims to assess the role of beta1-3 glucan supplementation in improving clinical symptoms and other outcomes amongst hospitalised patients with COVID-19.
Detailed Description
COVID-19 can present as a life-threatening disease characterised by respiratory failure and high circulating levels of inflammatory cytokines. Beta-glucans comprise a heterogeneous group of natural polysaccharides consisting of D-glucose monomers linked by a beta-glycosidic bond. They represent key structural elements of the cell wall and may serve as energy storage in bacteria, fungi including yeast, algae, and plants. In this triple-masked randomised trial, hospitalised patients requiring treatment with supplemental oxygen because of a laboratory-confirmed infection by SARS-CoV-2 will receive supplementation with 1-3 beta-glucans or placebo as part of their standard treatment. The primary endpoint of this trial is the intensity of clinical symptoms as detected by the Wisconsin Upper Respiratory Symptom Survey (WURSS). Patients requiring mechanical ventilation at baseline will be excluded, as will those with cognitive impairment that precludes the use of clinical assessment scales, patients in which an order to limit therapeutic efforts has been issued, pregnant or breastfeeding women and those who decline to participate in this study. Secondary outcomes will include clinical deterioration requiring admission to an intensive care unit, requirement of high-flow nasal cannula or invasive mechanical ventilation and overall survival. Patients will be followed-up until hospital discharge or up to fifteen days after randomisation. Statistical analyses will be undertaken by a statistician unaware of treatment allocation under the intention-to-treat principle.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
Keywords
beta-Glucans, Therapy, Signs and Symptoms, Mechanical ventilation, Inflammation, Survival

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Eligible participants will be randomised to receive either beta-glucan supplements or placebo for up to three days.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Beta-Glucans
Arm Type
Experimental
Arm Description
Patients allocated to this arm will receive MC 3x3, an oral supplement containing 25mg of 1,3 beta-Glucans daily for up to three consecutive days.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Participants allocated to this arm will receive a placebo that will be identical in form to the MC 3x3 pills used the interventional arm. These doses will be scheduled daily and administered orally for up to three consecutive days.
Intervention Type
Drug
Intervention Name(s)
MC 3x3
Intervention Description
Patients allocated to this arm will receive MC 3x3, an oral supplement containing 25mg of 1,3 beta-Glucans of fungal origin (Trichoderma sp.) daily for up to three consecutive days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Patients allocated to this arm will receive a matching placebo similar to MC 3x3 pills used in the intervention arm. Placebos will be delivered orally every day for up to three consecutive days.
Primary Outcome Measure Information:
Title
Symptom severity
Description
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Time Frame
WURSS-21 scores calculated 1 day after randomisation
Title
Symptom severity
Description
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Time Frame
WURSS-21 scores calculated 2 days after randomisation
Title
Symptom severity
Description
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Time Frame
WURSS-21 scores calculated 3 days after randomisation
Title
Symptom severity
Description
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Time Frame
WURSS-21 scores calculated 5 days after randomisation
Title
Symptom severity
Description
Symptom severity based on the Wisconsin Upper Respiratory Symptom Survey (WURSS) score.
Time Frame
WURSS-21 scores calculated 7 days after randomisation
Title
Symptom duration
Description
Total time with disease manifestations attributable to COVID-19.
Time Frame
Up to 2 weeks after randomisation or hospital discharge
Title
Clinical recovery
Description
Number of patients without clinical complaints attributable to COVID-19
Time Frame
Seven days after randomisation or up to hospital discharge
Secondary Outcome Measure Information:
Title
C-Reactive protein levels
Description
C-Reactive protein levels measured at various time intervals during the hospitalisation.
Time Frame
This laboratory exam will be measured on days 1, 3, 5 and 7 after randomisation.
Title
Absolute lymphocyte count
Description
Absolute lymphocyte counts measured at various time intervals during the hospitalisation.
Time Frame
This laboratory exam will be measured on days 1, 3, 5 and 7 after randomisation.
Title
Neutrophil to lymphocyte ratio
Description
Neutrophil to lymphocyte ratios measured at various time intervals during the hospitalisation.
Time Frame
This laboratory exam will be measured on days 1, 3, 5 and 7 after randomisation.
Title
Intensive Care Unit Admission
Description
Proportion of patients requiring admission to an intensive care unit in each study group
Time Frame
Up to seven days after randomisation
Title
Invasive mechanical ventilation
Description
Proportion of patients requiring invasive mechanical ventilation in each study group
Time Frame
Up to seven days after randomisation
Title
Survival
Description
Proportion of patients that survived COVID-19 in each study group
Time Frame
Up to seven days after randomisation
Title
Hospital Stay
Description
Total stay within the hospital amongst participants
Time Frame
Until hospital discharge
Other Pre-specified Outcome Measures:
Title
Adverse events
Description
Adverse events attributable to Beta-Glucan supplementation
Time Frame
Up to seven days after randomisation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult participants with an infection caused by SARS-CoV-2 confirmed with a reverse-transcription polymerase chain reaction (RT-PCR) obtained from a nasopharyngeal swab. Exclusion Criteria: Life expectancy < 6 months Currently receiving invasive mechanical ventilation at baseline. Cognitive impairment that precludes the use of WURSS or understanding the informed consent form. Refusal to participate.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Araya
Phone
989996955
Ext
+ 56 9
Email
michaelarayach@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Felipe T Martinez, MD, MSc
Phone
2573399
Ext
+56 32
Email
felipe.martinez@concentrainvestigacion.cl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alejandra Correa, MD
Organizational Affiliation
Hospital Geriátrico Paz de La Tarde
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Maria José Ruz
Organizational Affiliation
Hospital Gustavo Fricke
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mario Reyes
Organizational Affiliation
Science & Cash Group SpA
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Felipe Martinez, MD, MSc
Organizational Affiliation
Concentra Investigacion
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael Araya
Organizational Affiliation
Hospital Gustavo Fricke
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Gustavo Fricke
City
Viña Del Mar
State/Province
Valparaiso
ZIP/Postal Code
2570017
Country
Chile
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael Araya
Email
michaelarayach@gmail.com
First Name & Middle Initial & Last Name & Degree
Alejandra Correa, MD
Email
acorreall@gmail.com
First Name & Middle Initial & Last Name & Degree
Roberto A Merino, MD
First Name & Middle Initial & Last Name & Degree
Nicolas M Caroca, MD
First Name & Middle Initial & Last Name & Degree
Alejandra V Fernández, RN
First Name & Middle Initial & Last Name & Degree
Cristian Ortega, PharmD

12. IPD Sharing Statement

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Beta-glucans for Hospitalised Patients With COVID-19

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