Interferon Gamma Induced Protein 10 (IP-10) in a Clinical Decision Support Protocol in COVID-19 Patients
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ClinicalTrials.gov Identifier: NCT04389645 |
Recruitment Status :
Completed
First Posted : May 15, 2020
Last Update Posted : May 15, 2020
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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 |
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 |
- Diagnostic Test: IP-10 in CDS protocol
Dynamic IP-10 measurements in hospitalized COVID-19 positive patients
- IP-10 levels [ Time Frame: up to 24 months ]

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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 |
Inclusion Criteria:
- PCR- positive for COVID-19
Exclusion Criteria:
- <18 years of age

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
Israel | |
Rabin Medical Center | |
Petach Tikva, Israel |
Principal Investigator: | Shaul Lev, MD | Rabin Medical Center |
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 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |