Skip to content

Effect of Injectable Anticoagulants on Research for a Circulating Lupus-type Anticoagulant

Effect of Injectable Anticoagulants on Research for a Circulating Lupus-type Anticoagulant

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05416190
Acronym
ANTICOLA
Enrollment
188
Registered
2022-06-13
Start date
2022-06-02
Completion date
2024-05-21
Last updated
2024-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anticoagulant Drugs, Antiphospholipid Syndrome

Keywords

Lupus coagulation inhibitor, Anticoagulant drugs

Brief summary

The aim is to assess the effect of injectable anticoagulants (unfractionated heparin (UFH), low molecular weight heparins (LMWH), fondaparinux, danaparoid, argatroban) on lupus anticoagulant testing assays over broad anti-Xa activity ranges and to establish their potential for causing false-positive or false-negative results.

Detailed description

Citrated whole blood was collected from subjects with positive lupus anticoagulant (LA) testing and from subjects with negative LA testing. Injectable anticoagulants were prepared in demineralized water and added to plasma samples LA+ and LA- to obtain broad anti-Xa activity ranges. Anti-Xa measurement and LA testing were performed in neat and spiked plasma samples. LA testing was performed with 4 different analyzer-reagent combinations to represent almost all hemostasis manufacturers currently available. There will be no direct comparison between the LA+ and LA- groups, the objective is to evaluate the effect of increasing concentrations of injectable anticoagulants on these 2 distinct populations.

Interventions

DIAGNOSTIC_TESTLupus anticoagulant testing

The patient will have a visit during which a blood sample will be taken, a clinical examination will be performed, and data will be collected.

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Masking description

Patients are recruited according to their LA status (LA- or LA+).

Intervention model description

Citrated whole blood was collected from all participants and lupus anticoagulant testing was performed before and after spiking in vitro injectable anticoagulants. No distinction between the groups LA+ and LA-.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* For all subjects: * Adult male or female subject. * In capacity to give informed consent to participate in the research. * Affiliated to a Social Security system. For the LA- group: * Without a previous thrombosis and considered healthy on the basis of the interview and clinical examination. * Without coagulation disease For the LA+ group: \- Notion of the presence of lupus anticoagulant (according to ISTH criteria) and whose last test was positive.

Exclusion criteria

For all subjects: * Medical history considered by the investigator to be incompatible with the trial * Refused participation * Recent administration of oral or injectable anticoagulants * INR \> 1.5 * Pregnant women, nursing mothers * Guardianship, curatorship, deprived of liberty, safeguard of justice

Design outcomes

Primary

MeasureTime frameDescription
Results of lupus anticoagulant testing: positive or negativeday 1Concerning the impact of injectable anticoagulants on the final diagnosis of LA testing (negative or positive), in a population of LA+ and LA- subjects, particular attention will be paid to the study of false negatives and false positives expressed in % and 95% confidence intervals.

Secondary

MeasureTime frameDescription
Effect of injectable anticoagulants on the clotting times of each of the tests involved in LA testing (detection, mixing and confirmation tests).day 1comparison of clotting times in the absence and presence of increasing concentrations of anticoagulants will be carried out by Anova or non-parametric Kruskal-Wallis test if the conditions of Anova are not respected. Graphical representations will be associated with these analyses.
Determination of the threshold limits of injectable anticoagulants (anti-Xa activities) allowing a reliable LA diagnosis, for each analytical solution tested (analyzer/reagent combinations).day1comparison of clotting times in the absence and presence of increasing concentrations of anticoagulants will be carried out by Anova or non-parametric Kruskal-Wallis test if the conditions of Anova are not respected.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026