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Interferon Gamma Induced Protein 10 (IP-10) in a Clinical Decision Support Protocol in COVID-19 Patients

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04389645
Recruitment Status : Completed
First Posted : May 15, 2020
Last Update Posted : May 15, 2020
Sponsor:
Information provided by (Responsible Party):
MeMed Diagnostics Ltd.

Brief Summary:

The proposed project will pilot incorporation of rapid serial measurements of IP-10 into a CDS tool for moderate and severe COVID-19 patients.

The tool was applied to all comers with confirmed COVID-19 diagnosis at a secondary medical center in Israel.


Condition or disease Intervention/treatment
COVID-19 Diagnostic Test: IP-10 in CDS protocol

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Study Type : Observational
Actual Enrollment : 52 participants
Official Title: Interferon Gamma Induced Protein 10 (IP-10) in a Clinical Decision Support Protocol in COVID-19 Patients
Actual Study Start Date : April 7, 2020
Actual Primary Completion Date : May 12, 2020
Actual Study Completion Date : May 12, 2020

Intervention Details:
  • Diagnostic Test: IP-10 in CDS protocol
    Dynamic IP-10 measurements in hospitalized COVID-19 positive patients


Primary Outcome Measures :
  1. IP-10 levels [ Time Frame: up to 24 months ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
PCR-positive COVID-19 all comers
Criteria

Inclusion Criteria:

  • PCR- positive for COVID-19

Exclusion Criteria:

  • <18 years of age

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04389645


Locations
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Israel
Rabin Medical Center
Petach Tikva, Israel
Sponsors and Collaborators
MeMed Diagnostics Ltd.
Investigators
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Principal Investigator: Shaul Lev, MD Rabin Medical Center
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: MeMed Diagnostics Ltd.
ClinicalTrials.gov Identifier: NCT04389645    
Other Study ID Numbers: MM-5000-BV
First Posted: May 15, 2020    Key Record Dates
Last Update Posted: May 15, 2020
Last Verified: May 2020

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No