FHIR IG analytics| Package | hl7.fhir.uv.ebm |
| Resource Type | Evidence |
| Id | Evidence-6512.json |
| FHIR Version | R6 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
Generated Narrative: Evidence 6512
version: 3; Last updated: 2026-08-06 09:26:00+0000
ArtifactPublicationStatus: Active
url: https://fevir.net/resources/Evidence/6512
identifier: FEvIR Object Identifier/6512
name: OSFPreprint_PrimaryOutcomeMeasure_0_OutcomeAnalysis_0_BetweenGroupAnalysis_OG000_OG001
title: Percentage of Participants With Clinical Recovery Within 14 Days After Randomization Statistical Analysis for Nigella Sativa Oil vs Control in Nigella Sativa for COVID-19 OSF Preprint
citeAs:
Percentage of Participants With Clinical Recovery Within 14 Days After Randomization Statistical Analysis for Nigella Sativa Oil vs Control in Nigella Sativa for COVID-19 OSF Preprint [Database Entry: FHIR Evidence Resource]. Contributors: Brian S. Alper [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 6512. Revised 2021-07-19. Available at: https://fevir.net/resources/Evidence/6512. Computable resource at: https://fevir.net/resources/Evidence/6512#json.
status: Active
date: 2021-07-19 21:20:42+0000
author: Brian S. Alper:
publisher: Computable Publishing LLC
contact: support@computablepublishing.com
copyright:
https://creativecommons.org/licenses/by-nc-sa/4.0/
description:
This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.
variableDefinition
description:
Adult symptomatic patients with mild COVID-19 were recruited between May and August 2020 from King Abdulaziz University Hospital in Jeddah, Saudi Arabia.
variableRole: Population
observed: Group NCT04401202_Enrollment_Group
intended: NCT04401202 Eligibility Criteria
variableDefinition
description:
Nigella Sativa Oil (NSO)
variableRole: Exposure
observed: supplementation with oral capsules of NSO (MARNYS® Cuminmar 500 mg twice daily for 10 days) plus standard of care
variableDefinition
description:
Control
variableRole: Exposure
observed: standard of care medications alone
variableDefinition
description:
proportion of patients recovered (free of symptoms for 3 days) within 14 days after randomization
variableRole: Outcome
observed: Percentage of Participants With Clinical Recovery Within 14 Days After Randomization
statistic
description:
There were 47 patients in the treatment group (NSO) and 47 patients in the control group. The proportion of patients recovered in the treatment group was significantly higher than the control group, 37 (79%) versus 21 (45%) (p=0.001).
numberAffected: 58
SampleSizes
NumberOfStudies KnownDataCount 1 94 AttributeEstimates
Type Quantity P-value 0.001
{
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},
"text": {
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"div": "<!-- snip (see above) -->"
},
"extension": [
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"url": "https://fevir.net/resources/Evidence/6512",
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"value": "6512",
"assigner": {
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],
"name": "OSFPreprint_PrimaryOutcomeMeasure_0_OutcomeAnalysis_0_BetweenGroupAnalysis_OG000_OG001",
"title": "Percentage of Participants With Clinical Recovery Within 14 Days After Randomization Statistical Analysis for Nigella Sativa Oil vs Control in Nigella Sativa for COVID-19 OSF Preprint",
"citeAs": "Percentage of Participants With Clinical Recovery Within 14 Days After Randomization Statistical Analysis for Nigella Sativa Oil vs Control in Nigella Sativa for COVID-19 OSF Preprint [Database Entry: FHIR Evidence Resource]. Contributors: Brian S. Alper [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 6512. Revised 2021-07-19. Available at: https://fevir.net/resources/Evidence/6512. Computable resource at: https://fevir.net/resources/Evidence/6512#json.",
"status": "active",
"date": "2021-07-19T21:20:42.620Z",
"author": [
{
"name": "Brian S. Alper"
}
],
"publisher": "Computable Publishing LLC",
"contact": [
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"telecom": [
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"value": "support@computablepublishing.com"
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]
}
],
"copyright": "https://creativecommons.org/licenses/by-nc-sa/4.0/",
"description": "This Evidence Resource is referenced in an example for the EBMonFHIR Implementation Guide.",
"variableDefinition": [
{
"description": "Adult symptomatic patients with mild COVID-19 were recruited between May and August 2020 from King Abdulaziz University Hospital in Jeddah, Saudi Arabia.",
"variableRole": "population",
"observed": {
"reference": "Group/5224",
"type": "Group"
},
"intended": {
"reference": "Group/189713",
"type": "Group",
"display": "NCT04401202 Eligibility Criteria"
}
},
{
"description": "Nigella Sativa Oil (NSO)",
"variableRole": "exposure",
"observed": {
"display": "supplementation with oral capsules of NSO (MARNYS® Cuminmar 500 mg twice daily for 10 days) plus standard of care"
}
},
{
"description": "Control",
"variableRole": "exposure",
"observed": {
"display": "standard of care medications alone"
}
},
{
"description": "proportion of patients recovered (free of symptoms for 3 days) within 14 days after randomization",
"variableRole": "outcome",
"observed": {
"reference": "EvidenceVariable/5269",
"type": "EvidenceVariable",
"display": "Percentage of Participants With Clinical Recovery Within 14 Days After Randomization"
}
}
],
"statistic": [
{
"description": "There were 47 patients in the treatment group (NSO) and 47 patients in the control group. The proportion of patients recovered in the treatment group was significantly higher than the control group, 37 (79%) versus 21 (45%) (p=0.001).",
"numberAffected": 58,
"sampleSize": {
"numberOfStudies": 1,
"knownDataCount": 94
},
"attributeEstimate": [
{
"type": {
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/attribute-estimate-type",
"code": "C44185",
"display": "P-value"
}
]
},
"quantity": {
"value": 0.001
}
}
]
}
]
}