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Terminated No phase listed Observational Results available

ThRombosis ExclUsion STudy

ClinicalTrials.gov ID: NCT03477968

Public ClinicalTrials.gov record NCT03477968. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:22 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Primary objective: To demonstrate the ability of STA® - Liatest® D-Di XL combined with a clinical PreTest Probability (PTP) to safely exclude pulmonary embolism (PE) and deep venous thrombosis (DVT) as measured by Negative Predictive Value (NPV) and sensitivity. Secondary objectives: 1. To estimate additional STA® - Liatest® D-Di XL accuracy parameters, including specificity and positive predictive value (PPV) 2. To constitute a plasma bank to be used for future studies with other DDi assays under development by Stago.

Study identification

NCT ID
NCT03477968
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Diagnostica Stago
Industry
Enrollment
5,935 participants

Conditions and interventions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
Up to 79 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 25, 2018 (Actual)
Primary completion
Mar 29, 2023 (Actual)
Completion
Sep 5, 2024 (Actual)
Last update posted
Feb 25, 2025

2018 – 2024

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Yale New Haven Hospital New Haven Connecticut 06510 —
Northwestern Medical Center Chicago Illinois 60611 —
Indiana University Health Indianapolis Indiana 46202 —
Taylor regional Hospital Campbellsville Kentucky 42718 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Washington University St Louis Missouri 63110 —
Duke Hemostasis and Thrombosis Research Center Durham North Carolina 27710 —
Ohio State University Columbus Ohio 43210 —
Lehigh Hospital Allentown Pennsylvania 18103 —
St Luke's University Health Network Bethlehem Pennsylvania 18015 —
Jefferson University Hospital Philadelphia Pennsylvania 19107 —
UT Southwestern Dallas Texas 75390 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03477968, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 25, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03477968 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →