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| Column | Value |
|---|---|
| Trial registration number | NCT04980534 |
|
Full text link
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
|
|
First author
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
|
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Contact
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Not reported |
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Registration date
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
2021-07-28 |
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Recruitment status
Last imported at : Oct. 22, 2021, 10 a.m. Source : ClinicalTrials.gov |
Completed |
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Study design
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
RCT |
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Allocation
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Randomized |
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Design
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Parallel |
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Masking
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Open label |
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Center
Last imported at : March 15, 2023, 4 a.m. Source : ClinicalTrials.gov |
multi-center |
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Study aim
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Treatment |
|
Inclusion criteria
Last imported at : April 14, 2022, 11:30 p.m. Source : ClinicalTrials.gov |
the eligibility criteria for inclusion in the study were as follows: male and female hospitalized patients who have signed an informed consent. aged between 18-85 years old. rt-pcr confirmed covid-19. fever (over 37.2 celsius degrees). ct scan percentage area of lung involvement with ground-glass opacities < 50 %. respiratory rate < 20-30 /min spo2 ≥ 95%. the exclusion criteria were as follows: oxygen support (ventilation and non-invasive) uncompensated or exacerbated concomitant diseases or conditions that may complicate or make the patient's participation in the study impossible, or make it difficult to explain clinical findings. any known intolerability to any of the study regimens' components. patient's family or official relations with a member of staff of the clinical site. patient's failure to assess his/her physical and/or emotional condition. patient's failure to comply with the study requirements. patient's refusal to participate in the study. pregnancy or breastfeeding. |
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Exclusion criteria
Last imported at : April 14, 2022, 11:30 p.m. Source : ClinicalTrials.gov |
None |
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Number of arms
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
3 |
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Funding
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Catalysis SL |
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Inclusion age min
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
18 |
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Inclusion age max
Last imported at : April 14, 2022, 11:30 p.m. Source : ClinicalTrials.gov |
85 |
|
Countries
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Kazakhstan |
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Type of patients
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
Mild/moderate disease at enrollment |
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Severity scale
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
2: Mild/moderate disease at enrollment |
|
Total sample size
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
80 |
|
primary outcome
Last imported at : April 14, 2022, 11:30 p.m. Source : ClinicalTrials.gov |
Mean duration of hospitalization. |
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Notes
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
None |
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Phase
Last imported at : Nov. 16, 2021, 6:30 p.m. Source : ClinicalTrials.gov |
Not reported |
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Arms
Last imported at : July 29, 2021, noon Source : ClinicalTrials.gov |
[{"arm_notes": "", "treatment_id": 1737, "treatment_name": "Viusid", "treatment_type": "Nutrition", "pharmacological_treatment": "Non pharmacological treatment"}, {"arm_notes": "", "treatment_id": 125, "treatment_name": "Asbrip", "treatment_type": "Vitamins and dietary supplements", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "", "treatment_id": 2188, "treatment_name": "Standard of care", "treatment_type": "Standard of care", "pharmacological_treatment": "Standard of care"}] |