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QStat Cartridge in Obstetric Patients
NCT06255496 · View on ClinicalTrials.gov ↗
Study Summary
This study will assess the performance of the Quantra System with the QStat Cartridge versus standard of care coagulation testing in pregnant women at risk of bleeding at delivery.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Quantra Hemostasis Analyzer with the QStat Cartridge
Study Locations (6)
New York
- University of Rochester Medical Center — Rochester
Ohio
- Ohio State University Wexner Medical Center — Columbus
Oklahoma
- University of Oklahoma Medical Center — Oklahoma City
Pennsylvania
- Magee Womens Hospital — Pittsburgh
Texas
- Parkland Health — Dallas
Utah
- University of Utah — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 296 participants |
| Start Date | 2024-05-09 |
| Est. Completion | 2025-10-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06255496
The ClinicalTrials.gov registry entry for NCT06255496 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 296 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is HemoSonics, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Post Partum Hemorrhage appearing as the primary indexed condition, and to 1 intervention — of which Quantra Hemostasis Analyzer with the QStat Cartridge is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06255496 reports 6 study locations spanning 6 distinct geographic areas — top geographies include New York, Ohio, Oklahoma. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06255496 about?
NCT06255496 is a clinical study titled "QStat Cartridge in Obstetric Patients". This study will assess the performance of the Quantra System with the QStat Cartridge versus standard of care coagulation testing in pregnant women at risk of bleeding at delivery.
What is the current status of trial NCT06255496?
This trial is currently completed. The enrollment target is 296 participants. The study started on 2024-05-09. Estimated completion is 2025-10-30.
What conditions does trial NCT06255496 study?
This clinical trial studies the following conditions: Post Partum Hemorrhage, Blood Loss Massive. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06255496?
The interventions under investigation include: Quantra Hemostasis Analyzer with the QStat Cartridge (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06255496?
This trial is sponsored by HemoSonics, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06255496 being conducted?
This trial has 6 study locations across New York, Ohio, Oklahoma, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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