An Observational Cohort Trial of Outcomes and Antibody Responses Following Treatment With COVID19 Convalescent Plasma in Hospitalized COVID-19 Patients
Completed
Conditions studied: Covid19
In brief
This is an observational study designed to learn more about how COVID19 convalescent plasma works in patients with COVID19 compared to those patients who did not receive convalescent plasma treatment. Information about patient recovery will be collected from participants' electronic medical records to evaluate safety, clinical outcomes, and SARS-CoV2 antibody responses in patients who were treated with convalescent plasma under a separate expanded access protocol, NCT04372368.
Key facts
- Study ID
- NCT04471051
- Run by
- University of Colorado, Denver
- People needed
- 255
- Starts
- 2020-04-30
- Expected to finish
- 2020-08-20
- Last updated by the study team
- 2021-06-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18 years or older
- Hospitalized with COVID-19 respiratory symptoms and confirmation via COVID-19 SARS-CoV-2 RT-PCR testing.
- Patient treated with COVID19 convalescent plasma.
- Patient or surrogate designated decision maker is willing and able to provide written informed consent.
You may not qualify if…
- Receipt of pooled immunoglobulin in past 30 days
- Contraindication to transfusion or history of prior reactions to transfusion blood products
Where it is running
- Children's Hospital Colorado — Aurora, Colorado, United States
- University of Colorado Hospital — Aurora, Colorado, United States
- UCHealth Memorial Hospital North — Colorado Springs, Colorado, United States
- Denver Health Medical Center — Denver, Colorado, United States
- UCHealth Poudre Valley Hospital — Fort Collins, Colorado, United States
- UCHealth Highlands Ranch Hospital — Highlands Ranch, Colorado, United States
Full record on ClinicalTrials.gov
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