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Prevention of Infection and Incidence of COVID-19 in Medical Personnel Assisting Patients With New Coronavirus Disease

Primary Purpose

Increased Risk of SARS-CoV-2 Infection

Status
Completed
Phase
Phase 4
Locations
Russian Federation
Study Type
Interventional
Intervention
Bromhexine Hydrochloride
Sponsored by
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Increased Risk of SARS-CoV-2 Infection

Eligibility Criteria

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

Inclusion Criteria:

  1. Age of 18 years or more;
  2. Negative test (PCR) for SARS-CoV-2 infection;
  3. The absence of clinical manifestations of a respiratory infection;
  4. Contact with patients with laboratory and / or clinically confirmed SARS-CoV-2 infection;
  5. Signed informed consent to participate in the study.

Exclusion Criteria:

  1. Intolerance to Bromhexine hydrochloride;
  2. Work out of contact with SARS-CoV-2 infection;
  3. Non-compliance with the rules for the use of personal protective equipment when working with SARS-CoV-2 infection (the rules for the use of personal protective equipment in accordance with the recommendations of the Ministry of Health of Russia and the internal orders of the Director General of Almazov NMRC, relevant to the dates of research);
  4. Pregnancy and the period of breastfeeding;
  5. Other circumstances that the researcher considers inappropriate to participate in this study

Sites / Locations

  • Almazov National Medical Research Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Bromhexine hydrochloride Group

Control Group

Arm Description

medical personnel at risk for COVID-19 infection with oral administration of Bromhexine hydrochloride

medical personnel at risk for COVID-19 infection without oral administration of Bromhexine hydrochloride

Outcomes

Primary Outcome Measures

Negative Polymerase Chain Reaction (PCR)
Number of Participants with Negative PCR of SARS-CoV-2 and The Absence of Clinical Manifestations of COVID-19 Infection in individuals taking Bromhexine hydrochloride 4 weeks after randomization.

Secondary Outcome Measures

Number of Participants With Asymptomatic SARS-CoV-2 Infection
Number of Participants with Asymptomatic SARS-CoV-2 Infection
Number of Participants With Mild, Moderate and Severe COVID-19 Disease
number of participants with mild, moderate and severe COVID-19 disease
Number of Participants With Adverse Events
Number of Participants with Adverse Events

Full Information

First Posted
May 18, 2020
Last Updated
April 11, 2022
Sponsor
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
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1. Study Identification

Unique Protocol Identification Number
NCT04405999
Brief Title
Prevention of Infection and Incidence of COVID-19 in Medical Personnel Assisting Patients With New Coronavirus Disease
Official Title
Prevention of Infection and Incidence of COVID-19 in Medical Personnel Assisting Patients With New Coronavirus Disease: a Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
May 14, 2020 (Actual)
Primary Completion Date
August 9, 2020 (Actual)
Study Completion Date
August 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health

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 randomized controlled trial of the efficacy and safety evaluation of oral administration of Bromhexine hydrochloride for the prevention of SARS-CoV-2 infection and COVID-19 disease in medical personnel assisting patients with a new coronavirus disease
Detailed Description
This study aims to evaluate the oral administration of Bromhexine hydrochloride for the prevention of SARS-CoV-2 infection and COVID-19 disease in medical personnel assisting patients with a new coronavirus disease. The aim of the study is to determine the preventive role of this drug in the framework of reducing the incidence of coronavirus infection in risk groups (medical personnel). Several studies show, that the acute respiratory syndrome coronavirus SARS-CoV uses endosomal cysteine proteases cathepsin B and L (CatB/L) and the transmembrane protease serine type 2 (TMPRSS2) for the priming of the viral S-protein. The new coronavirus SARS-CoV-2 penetrates into alveolar epithelial type two cells through a similar mechanism. In detail, viral S-protein binds to pneumocyte angiotensin-converting enzyme 2 (ACE2) and then undergoes cleaving by TMPRSS2 in S1- and S2-subunits. This leads to the release of a fusion peptide, which allows the virus to enter the cell via endocytosis. Therefore, the protease TMPRSS2 can serve as a target for pharmacological agents to prevent the penetration of the SARS-CoV-2 into the cell. Bromhexine blocks the TMPRSS2 ability to activate a zymogen precursor of tissue plasminogen activator in vitro. Interestingly, TMPRSS2 is blocked by much lower concentrations then required to inactivate other proteases in the cell culture. However, these data cannot be simply extended to the clinical practice: whether the concentration of bromhexine in the lung tissue of properly treated patients would be enough to prevent the virus entry through the TMPRSS2-inactivation remains unclear. A randomized study in people at risk for coronavirus infection will clarify the role of Bromhexine hydrochloride as a prevention of this disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Increased Risk of SARS-CoV-2 Infection

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bromhexine hydrochloride Group
Arm Type
Experimental
Arm Description
medical personnel at risk for COVID-19 infection with oral administration of Bromhexine hydrochloride
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
medical personnel at risk for COVID-19 infection without oral administration of Bromhexine hydrochloride
Intervention Type
Drug
Intervention Name(s)
Bromhexine Hydrochloride
Intervention Description
Medical personnel at risk for COVID-19 infection will receive study medication for 14 days
Primary Outcome Measure Information:
Title
Negative Polymerase Chain Reaction (PCR)
Description
Number of Participants with Negative PCR of SARS-CoV-2 and The Absence of Clinical Manifestations of COVID-19 Infection in individuals taking Bromhexine hydrochloride 4 weeks after randomization.
Time Frame
4 weeks after randomization
Secondary Outcome Measure Information:
Title
Number of Participants With Asymptomatic SARS-CoV-2 Infection
Description
Number of Participants with Asymptomatic SARS-CoV-2 Infection
Time Frame
14 days after last contact
Title
Number of Participants With Mild, Moderate and Severe COVID-19 Disease
Description
number of participants with mild, moderate and severe COVID-19 disease
Time Frame
14 days after last contact
Title
Number of Participants With Adverse Events
Description
Number of Participants with Adverse Events
Time Frame
14 days after last contact

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age of 18 years or more; Negative test (PCR) for SARS-CoV-2 infection; The absence of clinical manifestations of a respiratory infection; Contact with patients with laboratory and / or clinically confirmed SARS-CoV-2 infection; Signed informed consent to participate in the study. Exclusion Criteria: Intolerance to Bromhexine hydrochloride; Work out of contact with SARS-CoV-2 infection; Non-compliance with the rules for the use of personal protective equipment when working with SARS-CoV-2 infection (the rules for the use of personal protective equipment in accordance with the recommendations of the Ministry of Health of Russia and the internal orders of the Director General of Almazov NMRC, relevant to the dates of research); Pregnancy and the period of breastfeeding; Other circumstances that the researcher considers inappropriate to participate in this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Evgeny Mikhaylov, MD, PhD
Organizational Affiliation
Almazov National Medical Research Centre
Official's Role
Study Director
Facility Information:
Facility Name
Almazov National Medical Research Centre
City
Saint Petersburg
ZIP/Postal Code
197341
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35103059
Citation
Mikhaylov EN, Lyubimtseva TA, Vakhrushev AD, Stepanov D, Lebedev DS, Vasilieva EY, Konradi AO, Shlyakhto EV. Bromhexine Hydrochloride Prophylaxis of COVID-19 for Medical Personnel: A Randomized Open-Label Study. Interdiscip Perspect Infect Dis. 2022 Jan 29;2022:4693121. doi: 10.1155/2022/4693121. eCollection 2022.
Results Reference
derived

Learn more about this trial

Prevention of Infection and Incidence of COVID-19 in Medical Personnel Assisting Patients With New Coronavirus Disease

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