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NCT01227005 · ClinicalTrials.gov registry record · Phase 4
Early Whole Blood in Patients Requiring Transfusion After Major Trauma
A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- Phase 4
- Development phase
- 107
- Enrollment target
NCT01227005: Completed Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
NCT01227005 is a Phase 4 study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 107 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01227005, a Phase 4 study, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 107 participants
- Enrollment target
Study Summary
The proposal will assess if patients who require massive transfusion can be accurately predicted early after emergency department arrival and assess if the use of stored whole blood during initial resuscitation will reduce transfusion needs compared to transfusion with component therapy and thus improve outcome.
Primary Outcome
Compare the ability of whole blood to reduce initial 24-hour transfusion requirements as compared to component therapy (red blood cells, plasma, and platelet units)
Interventions
- BIOLOGICAL Transfusion of blood products
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 107 participants |
| Start Date | 2011-05 |
| Est. Completion | 2012-12 |
| Phase | Phase 4 |
What the finished NCT01227005 record still lists
NCT01227005 is an interventional study that assigns participants to a tested intervention. The registered 107 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (79% lower).
The record links to 0 conditions, and to 1 intervention - of which Transfusion of blood products is the first listed.
NCT01227005 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01227005 about?
NCT01227005 is a clinical study titled "Early Whole Blood in Patients Requiring Transfusion After Major Trauma". The proposal will assess if patients who require massive transfusion can be accurately predicted early after emergency department arrival and assess if the use of stored whole blood during initial resuscitation will reduce transfusion needs compared to transfusion with component therapy and thus imp...
What is the current status of trial NCT01227005?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 107 participants. The study started on 2011-05. Estimated completion is 2012-12.
What interventions are being tested in trial NCT01227005?
The interventions under investigation include: Transfusion of blood products (BIOLOGICAL).
Who is sponsoring clinical trial NCT01227005?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01227005's enrollment target sits among peer trials
107 745th of 2000 higher than 1,254 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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