COVID Clinical Trial
Official title:
CRI and Continuous Assessment of Hemodynamic Compensation to Guide Fluid and Pressor Management in Severely Ill Patients With COVID-19
| NCT number | NCT04457817 |
| Other study ID # | 20-1406 |
| Secondary ID | |
| Status | Terminated |
| Phase | |
| First received | |
| Last updated | |
| Start date | December 1, 2020 |
| Est. completion date | April 8, 2021 |
| Verified date | November 2021 |
| Source | University of Colorado, Denver |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
The FDA has approved the CipherOx CRI T1 Tablet for use in subjects aged 19-36, and that this study aims to evaluate the device in subjects aged outside of this range and is being used off label. The FDA determined the Cipher OX CRI T1 Tablet to be a class II device in 2016, and additional research has been done since the FDA determination to further support the use of the device outside of its current labeling.
| Status | Terminated |
| Enrollment | 16 |
| Est. completion date | April 8, 2021 |
| Est. primary completion date | April 8, 2021 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 70 Years |
| Eligibility | Inclusion Criteria: Eligible patients will be those who are: - COVID-19 positive; - Ages > 18 and < 70 years old; - Require > 2 liters of oxygen by nasal cannula to maintain SpO2 > 90%; - Are admitted to the sixth floor at University Hospital, on one of two designated Hospitalist services (approximately 16 COVID-19 positive patients/service). Exclusion Criteria: - COVID-19 negative - Age <18 or >70 years - On <2 liters oxygen via nasal canula - Pregnant - Incarcerated - DNR/DNI - Decisionally Challenged |
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Colorado | Aurora | Colorado |
| Lead Sponsor | Collaborator |
|---|---|
| University of Colorado, Denver | Children's Hospital Colorado |
United States,
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* Note: There are 31 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Volume of IV fluid infused | Volume of IV fluid infused during treatment | 1 year | |
| Primary | Quantity of Blood pressure medication administered | Amount of blood pressure medication utilized during treatment | 1 year | |
| Primary | Resuscitation status | Categorical determination of resuscitation status as over- or under- resuscitated | 1 year | |
| Primary | FiO2 needs | FiO2 levels administered | 1 year | |
| Primary | Days on Oxygen | Days spent on oxygen | 1 year | |
| Primary | Number of participants with hospital acquired pneumonia | Number of participants with hospital acquired pneumonia | 1 year | |
| Primary | Number of Patients with Acute Kidney Injury (AKI) | Number of patients who acquire an acute kidney injury | 1 year | |
| Primary | Number of patients with hemodynamic collapse | Number of patients who experience hemodynamic collapse defined as drop in systolic blood pressure below 80mm Hg | 1 year | |
| Primary | mortality | Number of patients who experience mortality | 1 year |
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