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NCT06255496 · ClinicalTrials.gov registry record

QStat Cartridge in Obstetric Patients

A clinical trial of Post Partum Hemorrhage and Blood Loss Massive, sponsored by HemoSonics.

Completed
Registry status
296
Enrollment target
6
Study locations

NCT06255496 is a study of Post Partum Hemorrhage and Blood Loss Massive that has completed, run by HemoSonics. The registered enrollment target is 296 participants, below the 1,754-participant average among 7 other Post Partum Hemorrhage trials with a reported enrollment target (83% lower). The trial reports 6 study locations across 6 states.

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The verdict

NCT06255496, a study of Post Partum Hemorrhage and Blood Loss Massive, has completed, sponsored by HemoSonics.

COMPLETED
Registry status
296 participants
Enrollment target
6
Study locations

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.

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

FieldValue
Enrollment Target 296 participants
Start Date 2024-05-09
Est. Completion 2025-10-30

Sponsor

HemoSonics

24 total trials

What the Registry Record Tells You About NCT06255496

The ClinicalTrials.gov registry entry for NCT06255496 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 296 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,754-participant average among 7 other Post Partum Hemorrhage trials with a reported enrollment target (83% lower). The listed sponsor is HemoSonics, which has 24 total studies on file at ClinicalTrials.gov.

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.

NCT06255496 reports 6 study locations spanning 6 distinct geographic areas - top geographies include New York, Ohio, Oklahoma.

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.

What interventions are being tested in trial NCT06255496?

The interventions under investigation include: Quantra Hemostasis Analyzer with the QStat Cartridge (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT06255496?

This trial is sponsored by HemoSonics, which has 24 total clinical trials registered on ClinicalTrials.gov.

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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.