Clinical trial Recruiting at 1 site Observational Ages 18 and up

Registry of patients with antiphospholipid antibodies

Official title: Constitution d'Une Collection d'Echantillons Biologiques Associee a Une Base de Donnees de Patients Possedant Des Anticorps Antiphospholipides

Run by Central Hospital, Nancy, France · NCT04308564 · Data updated 2026-11-12

This study is creating a registry to track adults with antiphospholipid antibodies to better understand their health and gather important information over time.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorCentral Hospital, Nancy, France
Academic / other
Locations2 sites (Lille and 1 other locations)
StatusRecruiting
StartedApril 12, 2021
Main results expectedApril 1, 2030
Study endsApril 1, 2031
Registry record updatedDecember 20, 2021
Trial IDNCT04308564 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 to 60 who have persistent positivity for antiphospholipid antibodies.

Probably not a fit

Patients who are pregnant or unable to provide informed consent will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to create a comprehensive registry for patients who test positive for antiphospholipid antibodies. Utilizing a web-based application called REDCap, the study collects data on patient demographics, clinical characteristics, and laboratory results related to antiphospholipid syndrome. Eligible participants are adults aged 18 to 60 who have shown persistent positivity for specific antiphospholipid antibodies. Patients will be monitored annually for clinical updates and blood samples will be collected for further analysis.

Why it matters

Potential benefit: If successful, this registry could enhance understanding of antiphospholipid syndrome and improve patient management.

How similar studies have gone: While this approach is observational and builds on existing knowledge, similar registries have shown success in improving patient outcomes in related conditions.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* age between 18 and 60 years;
* persistent (at least 12 weeks apart) aPL-positivity within 12 months prior to screening

Exclusion Criteria:

* no inform consent
* impossible follow up
* pregnancy

Where it's running

  • CHRU de Nancy
    Nancy, France
    Recruiting
  • CHRU de Lille
    Lille, France
    Not yet recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.