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Silymarin in COVID-19 Patients Admitted to Hospital With Elevated Liver Enzymes (SILCOVINT-21)

Primary Purpose

Covid19, Liver Diseases

Status
Completed
Phase
Phase 4
Locations
Slovakia
Study Type
Interventional
Intervention
Silymarin
Sponsored by
F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring COVID-19, In-hospital mortality, Internal medicine

Eligibility Criteria

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

Inclusion Criteria:

  • consecutive, adult, admitted to an internal medicine ward with internistic diagnosis, together with COVID-19, and elevated liver enzymes (any of AST, ALT, GGT, ALP), provided written informed consent

Exclusion Criteria:

  • too sick - terminal illness (no potential for recovery); critical condition on admission requiring immediate tracheal intubation; or any extra-pulmonary organ failure; completely vaccinated against COVID19.

Sites / Locations

  • F.D.Roosevelt Teaching Hospital
  • University Hospital Bratislava

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

LAGOSA ARM

Control arm

Arm Description

Consecutively admitted patients will be allocated silymarin tablets (150 mg each) T.I.D. 3-2-2

Consecutive patients with the same inclusion/exclusion criteria as in active arm, hospitalised at the same department before the initiation of the study (historical controls)

Outcomes

Primary Outcome Measures

Improvement in the COVID-19 stage of at least 1 point
Evolution of COVID-19 will be recorded according to a WHO criteria and reported as worsening (including death) / no change / improvement
Improvement in the activity of aminotranspherases
Change in the level of ALT

Secondary Outcome Measures

Improvement in the diabetes control
Change in the glycemia
Improvement in the blood inflammatory markers
Change in C-reactive protein levels
Improvement in the dyspnea
Improvement of at least one point in the NYHA classification
Improvement in the acute kidney injury
Any improvement in the serum creatinine level
Improvement in the blood inflammatory markers
Improvement in the interleukin - 6 level

Full Information

First Posted
March 19, 2021
Last Updated
August 2, 2022
Sponsor
F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica
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1. Study Identification

Unique Protocol Identification Number
NCT04816682
Brief Title
Silymarin in COVID-19 Patients Admitted to Hospital With Elevated Liver Enzymes
Acronym
SILCOVINT-21
Official Title
Does Silymarin Mitigate Clinical Course of COVID-19 in Patients Admitted to an Internal Medicine Ward With Elevated Liver Enzymes?
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
March 17, 2021 (Actual)
Primary Completion Date
June 30, 2021 (Actual)
Study Completion Date
December 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica

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
Of patients admitted to an internal medicine ward with internistic diagnosis/es together with COVID-19, substantial proportion has elevated liver enzymes. silymarin / silibinin (milk thistle extract) has been approved as an add-on therapy in various acute and chronic liver diseases; moreover, there is evidence to suggest that it's dual effect (anti-viral and immune-modulatory) might be of benefit in patients infected with SARS-CoV-2. As there is no effective/approved pharmacotherapy for COVID-19, a pilot study with Silymarine in hospitalised patients has been undertaken
Detailed Description
According to the Bosch-Barrera et al. paper of 2021, silibinin in a daily dose of more than 1000 mg could improve clinical course of COVID-19 by its dual action: 1.direct inhibition of SARS-CoV-2 replication as well as 2.modulation of innate immune response - 2a. its initial (hyper)inflammation as well as 2b. later reparative phase, respectively. Moreover, the drug is known for its safety and has been approved and widely used in the region for liver diseases. Therefore, the investigation was set out to determine the efficacy of silymarin (compound closely related to Silibinin which is available in the region) in improving the outcome of a liver disease and of COVID-19, respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Liver Diseases
Keywords
COVID-19, In-hospital mortality, Internal medicine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Sequential Assignment
Model Description
Prospective open label study using historical cohort for propensity-match analysis
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LAGOSA ARM
Arm Type
Active Comparator
Arm Description
Consecutively admitted patients will be allocated silymarin tablets (150 mg each) T.I.D. 3-2-2
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Consecutive patients with the same inclusion/exclusion criteria as in active arm, hospitalised at the same department before the initiation of the study (historical controls)
Intervention Type
Drug
Intervention Name(s)
Silymarin
Other Intervention Name(s)
LAGOSA
Intervention Description
Silymarine tablets will be provided irrespective of meal by a registered nurse T.I.D
Primary Outcome Measure Information:
Title
Improvement in the COVID-19 stage of at least 1 point
Description
Evolution of COVID-19 will be recorded according to a WHO criteria and reported as worsening (including death) / no change / improvement
Time Frame
During the hospital stay - up to around 21 days
Title
Improvement in the activity of aminotranspherases
Description
Change in the level of ALT
Time Frame
During the hospital stay - up to around 21 days
Secondary Outcome Measure Information:
Title
Improvement in the diabetes control
Description
Change in the glycemia
Time Frame
During the hospital stay - up to around 21 days
Title
Improvement in the blood inflammatory markers
Description
Change in C-reactive protein levels
Time Frame
During the hospital stay - up to around 21 days
Title
Improvement in the dyspnea
Description
Improvement of at least one point in the NYHA classification
Time Frame
During the hospital stay - up to around 21 days
Title
Improvement in the acute kidney injury
Description
Any improvement in the serum creatinine level
Time Frame
During the hospital stay - up to around 21 days
Title
Improvement in the blood inflammatory markers
Description
Improvement in the interleukin - 6 level
Time Frame
During the hospital stay - up to around 21 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: consecutive, adult, admitted to an internal medicine ward with internistic diagnosis, together with COVID-19, and elevated liver enzymes (any of AST, ALT, GGT, ALP), provided written informed consent Exclusion Criteria: too sick - terminal illness (no potential for recovery); critical condition on admission requiring immediate tracheal intubation; or any extra-pulmonary organ failure; completely vaccinated against COVID19.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lubomir SKLADANY, MD, PhD
Organizational Affiliation
Study Principal Investigator F.D.Roosevelt Teaching Hospital, Banska Bystrica, Slovakia
Official's Role
Principal Investigator
Facility Information:
Facility Name
F.D.Roosevelt Teaching Hospital
City
Banska Bystrica
ZIP/Postal Code
97401
Country
Slovakia
Facility Name
University Hospital Bratislava
City
Bratislava
ZIP/Postal Code
82101
Country
Slovakia

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Complete dataset will be shared on request under GDPR rules
IPD Sharing Time Frame
Dataset / protocol / ICF will be open for audit anytime Dataset will be shared after completion of upload
IPD Sharing Access Criteria
Journal editors Investigators - by the hypothesis testable on the dataset Auditing authority
IPD Sharing URL
http://www.fnspfdr.sk
Citations:
PubMed Identifier
32517353
Citation
Bosch-Barrera J, Martin-Castillo B, Buxo M, Brunet J, Encinar JA, Menendez JA. Silibinin and SARS-CoV-2: Dual Targeting of Host Cytokine Storm and Virus Replication Machinery for Clinical Management of COVID-19 Patients. J Clin Med. 2020 Jun 7;9(6):1770. doi: 10.3390/jcm9061770.
Results Reference
result

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Silymarin in COVID-19 Patients Admitted to Hospital With Elevated Liver Enzymes

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