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HemorrhageQASHNCT07105904

Biological and Clinical Relevance of Quantra Viscoelastic Hemostatic Assay in Hemorrhagic Cardiac Surgery

An observational study of Hemorrhage and Cardiac Surgery, run by Pitié-Salpêtrière Hospital at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this observational study is to assess the correlation between Quantra viscoelastometric assay and laboratory hemostasis biology in a cardiac surgery cohort presenting with acute hemorrhage in the operating room. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hemorrhage, Cardiac Surgery, Hemorrhagic Shock
What is being tested?
Viscoelastometric hemostatic assay
How many people
600 participants
Where
1 siteFrance
Study dates
10 Jul 2025to 15 Mar 2026
How long will I take part?
1 Month
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Monocentric prospective population of consecutive patients undergoing cardiac surgery with cardiopulmonary bypass

Who may be able to join

  • cardiac surgery with cardiopulmonary bypass, either scheduled or urgent
  • adult patient
  • hemostatic assay including Quantra and standard biology (PT, ACT, fibrinogen concentration and platelet count) at cardiopulmonary bypass weaning (post-protamine)

Who cannot join

  • non-opposition for participation not collected

Trial locations and contacts

1 site in 1 country.

France1 site
  • Pitié-Salpêtrière Hospital

    Paris, 75013

Other trials in France

About this study

Official title: Biological and Clinical Relevance of Quantra Viscoelastic Hemostatic Assay in Hemorrhagic Cardiac Surgery: a Prospective Observational Study

The goal of this observational study is to assess the correlation between Quantra viscoelastometric assay and laboratory hemostasis biology in a cardiac surgery cohort presenting with acute hemorrhage in the operating room. The main questions it aims to answer are:

  • is Quantra a valuable surrogate for hemostasis biology in the setting of bleeding cardiac surgery?
  • are Quantra parameters well correlated with tranfusion thresholds in the setting of bleeding cardiac surgery?
Read the detailed description

This observational study aims to assess the relevance of Quantra use in the setting of cardiac surgery patients presenting with acute bleeding in the operating room.

Hemorrhage is frequent in cardiac surgery. In the setting of per-operative acute bleeding, patient management and transfusions require a meticulous approach as both under-treatment and over-treatment can concur to morbidity and mortality. In this specific setting, the short timeframe of management usually does not allow usual laboratory tests (prothrombin time, activated clotting time, fibrinogen and platelets counts) to be integrated in the decision-making process. Viscoelastic hemostatic assays (VHA) such as Quantra might be relevant in this setting, owing to point-of-care bedside features.

As part of usual care for patients undergoing cardiopulmonary bypass for cardiac surgery at the Pitié-Salpêtrière Hospital, the investigators use Quantra viscoelastometric tests in various situations , including for per-operative hemorrhage management. Yet, it appears Quantra relevance has never been challenged in this population.

The investigators seek to determine whether in a population of patients presenting with significant hemorrhage in the operating room of cardiac surgery Quantra parameters (CT, CTH, FCS and PCS) are well-correlated to standard biology testing (prothrombin time, activated clotting time, fibrinogen and platelets count) and to transfusion thresholds.

Universal Definition of Perioperative Bleeding (UDPB) is a widely used quantification of bleeding in cardiac surgery. Nonetheless, most of its parameters of interest are assessed post-operatively and definition of acute bleeding during cardiac surgery lack. The investigators propose different bleeding definitions to assess hemorragic intra-operative events: 5 or more labile blood products transfused after protamine administration, and a modified UDPB definition to properly match significant per-operative bleeding events. The modified UDPB definition of interest will classify patients presenting with severe hemorrhage, patients presenting with massive hemorrhage as following:

Severe hemorrhage will be defined when one or more of the following occur:

  • no sternal closure or use of a modified closure strategy (such as GoreTex closure)
  • use of 5 to 10 blood products (packed red blood cells (RBC), fresh frozen plasma (FFP), platelets) during surgery
  • more than 4.5g of fibrinogen cryoprecipitate or concentrate administered during surgery
  • more than 50 UI/kg of human prothrombin complex (PPSB) administered during surgery
  • three different hemostatic products within FFP, platelets, fibrinogen products and PPSB administered during surgery
  • re-infusion of more than 1000mL of blood recovered from cell-salvage process

Massive hemorrhage will be defined as one or more of the following:

  • use of more than 10 blood products (RBC, FFP, platelets) during surgery
  • use of recombinant activated factor VII during surgery
  • use of all hemostatic products available (FFP, platelets, PPSB, fibrinogen products).

This study is conducted in accordance with French law pending to observational studies. Non-opposition of patients is assessed prior to inclusion and data collection. Registry datas are extracted from the patients's medical records after anonymization.

Sample size has been estimated considering that 70 patients with acute bleeding in the operating room will be needed to properly assess correlation between Quantra and hemostasis biology in this population of interest. Considering a 15% incidence of bleeding in the hospital, 600 patients should be included overall to attain this objective. Yearly, 1200 to 1300 patients undergo cardiopulmonary bypass for cardiac surgery at the Pitié-Salpêtrière hospital. Quantra viscoelastometric assay and hemostasis biology are part of usual care and are usually tested when weaning cardiopulmonary bypass (i.e. after protamin antagonization) when risk factors for bleeding are present. Considering Quantra consumption from previous years (>1000/y in 2023 and 2024), although multiple testing is possible for some bleeding patients, the investigators estimate that about half of the patients are tested for both Quantra and hemostasis biology at the time of weaning from CPB. Hence, it is planned to include prospective patients undergoing cardiac surgery with CPB for 1 year.

Statistical analysis will be computed by the investigators. Results for categorical variables, expressed as number (%), will be compared using the χ² test or Fisher's exact test when appropriate. Continuous variables, expressed as mean (± standard deviation) or median [25th-75th percentile interquartile range (IQR)], will be compared using Student's t-test or Wilcoxon's rank-sum test, depending on data distribution. Missing datas will be excluded from statistical analysis. Correlations between Quantra parameters and Prothrombin Time, Activated Clotting Time, fibrinogen count and platelet counts will be analyzed by Spearman-Rank test. Statistical association between Quantra parameters and transfusion thresholds will be assessed by Receiver Operating Characteristics (ROC) curves and extraction of best thresholds with Youden points.

Being tested
Viscoelastometric hemostatic assay
Keywords
hemmorhage, hemorrhagic cardiac surgery, Quantra, viscoelastometric assay, cardiac surgery
Medical subject headings
Hemorrhage, Shock, Hemorrhagic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Viscoelastometric hemostatic assayDiagnostic test

    Also called Quantra

    As part of usual care, when weaning the patient from CPB during cardiac surgery, blood samples are withdrawn from the patient to assess hemostasis: we test both Quantra viscoelastometric assay and biological hemostasis including QT, ACT, fibrinogen and platelet count

Study groups in NCT07105904
Study groupRoleWhat they receive
Monocentric consecutive patients undergoing cardiac surgeryMonocentric consecutive patients undergoing cardiac surgery, tested for biological hemostasis during surgery with both viscoelastometric assay (Quantra Qplus) and QT, ACT, fibrinogenemia, platelet count.
Receives: Diagnostic Test: Viscoelastometric hemostatic assay

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Correlation of Quantra with Prothrombin Time and Activated Clotting Time in patients presenting with acute bleeding in the operating room

    In the subgroup of patients presenting with either severe or massive hemorrhage as defined previously: correlation between Clotting Time without or with Heparinase (CT / CTH) with Prothrombin Time (PT) and Activated Clotting Time (ACT), all measured in seconds

    Measured: From enrollment to 1 month post-operatively

  2. Correlation of Quantra with fibrinogen concentration in patients presenting with acute bleeding in the operating room

    In the subgroup of patients presenting with either severe or massive hemorrhage as defined previously: correlation between Fibrinogen contribution to Clot Stiffness (FCS), in hPa, and patient's blood fibrinogen concentration in g/L

    Measured: From enrollment to 1 month post-operatively

  3. Correlation of Quantra with platelet count in patients presenting with acute bleeding in the operating room

    In the subgroup of patients presenting with either severe or massive hemorrhage as defined previously: correlation between Platelet contribution to Clot Stiffness (PCS), in hPa, and patient's platelet count in G/L

    Measured: From enrollment to 1 month post-operatively

Secondary outcomes (6)
  1. Correlation of Quantra with Prothrombin Time (PT) and Activated Clotting Time (ACT) in patients without bleeding

    In the subgroup of patients not presenting with acute bleeding in the operating room: correlation between Clotting Time without or with Heparinase (CT / CTH) with Prothrombin Time (PT) and Activated Clotting Time (ACT), all measured in seconds

    Measured: From enrollment to 1 month post-operatively

  2. Correlation of Quantra with fibrinogen concentration in patients without bleeding

    In the subgroup of patients not presenting with acute bleeding in the operating room: correlation between Fibrinogen contribution to Clot Stiffness (FCS), in hPa, and patient's blood fibrinogen concentration in g/L

    Measured: From enrollment to 1 month post-operatively

  3. Correlation of Quantra with platelet count in patients without bleeding

    In the subgroup of patients not presenting with acute bleeding in the operating room: correlation between Platelet contribution to Clot Stiffness (PCS), in hPa, and patient's platelet count in G/L

    Measured: From enrollment to 1 month post-operatively

  4. Correlation between Quantra and prothrombin time transfusion threshold in patients presenting with hemorrhage in cardiac surgery

    In the subgroup of patients presenting with either severe or massive hemorrhage as defined previously: correlation between Clotting Time without or with Heparinase (CT / CTH) and Prothrombin Time < 50%

    Measured: From enrollment to 1 month post-operatively

  5. Correlation between Quantra and fibrinogen concentration transfusion thresholds in patients presenting with hemorrhage in cardiac surgery

    In the subgroup of patients presenting with either severe or massive hemorrhage as defined previously: correlation between Fibrinogen contribution to Clot Stiffness (FCS), in hPa, and patient's blood fibrinogen concentration <1.5g/L

    Measured: From enrollment to 1 month post-operatively

  6. Correlation between Quantra and platelet count transfusion thresholds in patients presenting with hemorrhage in cardiac surgery

    In the subgroup of patients presenting with either severe or massive hemorrhage as defined previously: correlation between Platelet contribution to Clot Stiffness (PCS), in hPa, and patient's platelet count <50G/L

    Measured: From enrollment to 1 month post-operatively

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Aug 2025
  2. Study start10 Jul 2025
  3. Primary completion15 Feb 2026
  4. Study completion15 Mar 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
600 participants (actual)
Target duration
1 Month
IDs, dates and publications
ClinicalTrials.gov ID
NCT07105904
Sponsor's protocol ID
IRB 00010254 - 2025 - 065
Acronym
QASH
Status last verified
Apr 2026
First submitted
21 Jul 2025
Last updated
20 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
Yes: All collected IPD

Publications

  • Dyke C, Aronson S, Dietrich W, Hofmann A, Karkouti K, Levi M, Murphy GJ, Sellke FW, Shore-Lesserson L, von Heymann C, Ranucci M. Universal definition of perioperative bleeding in adult cardiac surgery. J Thorac Cardiovasc Surg. 2014 May;147(5):1458-1463.e1. doi: 10.1016/j.jtcvs.2013.10.070. Epub 2013 Dec 9.

    PubMed 24332097
  • Naik BI, Tanaka K, Sudhagoni RG, Viola F. Prediction of hypofibrinogenemia and thrombocytopenia at the point of care with the Quantra(R) QPlus(R) System. Thromb Res. 2021 Jan;197:88-93. doi: 10.1016/j.thromres.2020.11.008. Epub 2020 Nov 10.

    PubMed 33197797
  • Huffmyer JL, Fernandez LG, Haghighian C, Terkawi AS, Groves DS. Comparison of SEER Sonorheometry With Rotational Thromboelastometry and Laboratory Parameters in Cardiac Surgery. Anesth Analg. 2016 Dec;123(6):1390-1399. doi: 10.1213/ANE.0000000000001507.

    PubMed 27749339
  • Achneck HE, Sileshi B, Parikh A, Milano CA, Welsby IJ, Lawson JH. Pathophysiology of bleeding and clotting in the cardiac surgery patient: from vascular endothelium to circulatory assist device surface. Circulation. 2010 Nov 16;122(20):2068-77. doi: 10.1161/CIRCULATIONAHA.110.936773. No abstract available.

    PubMed 21098468

Questions about this trial

What is this clinical trial studying?

An observational study of Hemorrhage and Cardiac Surgery, run by Pitié-Salpêtrière Hospital at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Correlation of Quantra with Prothrombin Time and Activated Clotting Time in patients presenting with acute bleeding in the operating room (time frame: From enrollment to 1 month post-operatively). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07105904, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Apr 2026.

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