Safe and Timely Antithrombotic Removal (STAR) Registry
← catalyst calendarSponsored by CytoSorbents, Inc (industry) · CTSO — their whole pipeline →.
Phase
—
Status
Recruiting
Study type
Observational
Enrollment
1,000estimated
Sites
30
Countries
Austria, Belgium, Germany +3
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2021-09-30 | actual | When the study began enrolling |
| Primary completion | 2025-09-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-09-30 | estimated | The whole study's end, after follow-up |
| First posted | 2021-10-14 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-07-16 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Hemorrhage, Surgical
- Hemorrhage Postoperative
- Blood Loss, Surgical
- Blood Loss, Postoperative
Intervention
- Device: CytoSorb
Primary outcome
what the primary-completion date above is the date OFBleeding complications including requirements for transfusions and other blood products
measured Assessed until postoperative day (POD) 3, date of ICU discharge, or date of death, whatever comes first; on average 3 days
Publications
- PMID 38709456 — reports results
- PMID 40933270 — linked by the registry
- PMID 40044567 — linked by the registry
- PMID 39833891 — linked by the registry
Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.
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