Trials / Completed
CompletedNCT07490314
Blood Product Supply
Blood Product Supply During COVID-19
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- Methodist Health System · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Data about the links between Coronavirus disease 2019(COVID-19) and the safety of blood products during the pandemic is inadequate. During the COVID-19 pandemic, high volumes of patients receiving blood products due to post-terminal surgical complications depleted stores for the entire hospital, resulting in surgeons unable to acquire emergent blood products. Data from this study can be used to develop a policy on how to handle blood shortage issues during this and future pandemics. Also, this data can be used to determine future policies on use of blood products from COVID-19-positive donors.
Detailed description
* To identify the circumstances associated with observed delays in receiving blood products to use in emergent cases. * Determine the cost/benefit of moribund patients receiving massive transfusion during the COVID-19 pandemic. * Quantify COVID-19 diagnosis and complications in patients arriving with no indication of disease at index admission as relative to in hospital or blood product exposure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Document delays and frequencies of inadequate blood products for emergent cases | The COVID-19 pandemic is contributing to delays in blood product acquisition and inadequate blood product supplies for emergent cases in hospitals |
Timeline
- Start date
- 2020-03-01
- Primary completion
- 2021-03-21
- Completion
- 2025-06-25
- First posted
- 2026-03-24
- Last updated
- 2026-03-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT07490314. Inclusion in this directory is not an endorsement.