CONTAIN COVID-19: Convalescent Plasma to Limit COVID-19 Complications in Hospitalized Patients
Completed · Phase 2 · Has a placebo group
Conditions studied: COVID-19, Coronavirus, Coronavirus Infection
In brief
This is a randomized, blinded phase 2 trial that will assess the efficacy and safety of anti-SARS-CoV-2 convalescent plasma in hospitalized patients with acute respiratory symptoms requiring oxygen supplementation.
Key facts
- Study ID
- NCT04364737
- Run by
- NYU Langone Health
- People needed
- 941
- Starts
- 2020-04-17
- Expected to finish
- 2022-12-12
- Last updated by the study team
- 2023-01-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients ≥18 years of age
- Hospitalized with laboratory confirmed COVID-19
- One or more of the following respiratory signs or symptoms: cough, chest pain, shortness of breath, fever, oxygen saturation ≤ 94%, abnormal CXR/CT imaging)
- Hospitalized for ≤ 72 hours OR within day 3 to 7 days from first signs of illness
- On supplemental oxygen, non-invasive ventilation or high-flow oxygen
- Patients may be on other randomized controlled trials of pharmaceuticals for COVID -19 and patients who meet eligibility criteria will not be excluded on this basis.
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
- Invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO)
- Volume overload secondary to congestive heart failure or renal failure
- Unlikely to survive past 72 hours from screening based on the assessment of the investigator
- Unlikely to be able to assess and follow outcome due to poor functional status
Where it is running
- Yale University School of Medicine — New Haven, Connecticut, United States
- University of Miami Hospital and Clinics — Miami, Florida, United States
- NYU Langone Health — New York, New York, United States
- Montefiore Medical Center — The Bronx, New York, United States
- University of Texas Rio Grande Valley — Edinburg, Texas, United States
- The University of Texas Health Science Center — Houston, Texas, United States
- The University of Texas Health Science Center — Tyler, Texas, United States
- Aurora St. Luke's Medical Center — Milwaukee, Wisconsin, United States
- Medical College of Wisconsin / Froedtert Memorial Lutheran Hospital — Milwaukee, Wisconsin, United States
Full record on ClinicalTrials.gov
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