NCT06100718Recrutement en cours
Discovery of New Cancer in the 1-year Follow-up After Ischemic Stroke in Patients at Risk: The INVISIBLE-1 Study
Résumé
INVISIBLE-1 aims to prospectively follow patients up to one year after ischemic stroke to: 1. Determine the cumulative incidence of occult cancer in patients with embolic stroke of undetermined source (ESUS) and elevated D-dimer 2. Describe occult cancer characteristics and spontaneous course of occult cancer Methodology The investigators will include 370 stroke patients with elevated D-dimer (≥ 820 μg/L) at the time of stroke, suspicion of ESUS after initial workup and without known cancer. The investigators will perform a follow-up telephone interview at one year to assess the occurrence of a new cancer and characterize the course of the disease. Significance Determining the real incidence of occult cancer in high-risk patients will help support the implementation of screening trials in the future. Faster detection and treatment of occult cancers would significantly impact patient' outcomes by offering faster cancer treatment and optimal secondary stroke prevention.
Critères d'inclusion
• Informed consent as documented by signature from patient or next of kin • Age ≥ 18 years old • Acute ischemic stroke with symptom onset within 48 h before admission • Acute ischemic stroke with: • persistent signs and symptoms of stroke lasting for ≥ 24 hours OR • acute brain infarction documented by computer tomography (CT) or MRI • D-dimer ≥ 820 μg/L measured after symptom-onset and within 24h after admission • Embolic stroke of unknown source (ESUS)* after initial work-up (acute cerebral imaging, 12-lead electrocardiogram, cardiac monitoring for at least 24h and echocardiography)
Critères d'exclusion
• Active cancer** known at time of index-stroke • Intravenous Thrombolysis administrated prior to D-dimer measurement: Use of external laboratory value possible if available • New diagnosis of central nervous system cancer • Patient or next of kin (in case of lacking capacity) unlikely to be compliant or available for study follow-up interview ESUS*: According to the definition from the NAVIGATE ESUS randomized trial: Non-lacunar ischemic stroke occurring in a patient in whom investigations did not show another specifically treatable underlying stroke etiology, primarily \>50% stenosis in a proximal extracranial or intracranial artery, atrial fibrillation, other major-risk cardioembolic sources, or other determined etiology. Active Cancer**: According to the definition from the International Society on Thrombosis and Haemostasis: Cancer diagnosed within the previous six months, recurrent, regionally advanced or metastatic cancer, cancer for which treatment had been administered within six months, or hematological malignancy that is not in complete remission for more than 5 years. ► Patients with history of cancer not meeting these criteria anymore can be included in the study.
Contacts
Les coordonnées de l'équipe de l'essai s'affichent sur demande.
Voir la fiche officielle de l'essai- Statut
- Recrutement en cours
- Phase
- —
- Type d'étude
- Observationnelle
- Pays
- Suisse
- Promoteur
- Insel Gruppe AG, University Hospital Bern(Autre)
- N° de protocole
- 2021-01797
- Pathologies
- Cancer-related Stroke, Paraneoplastic Coagulopathy, Occult Cancer, Ischemic Stroke, Embolic Stroke of Undetermined Source, D-dimer
- Interventions
- —
Lieux · 3
- Lausanne, SuisseDept. of Neurology, Centre Hospital Universitaire VaudoisRecrute dans ce centre
- Basel, SuisseDept. of Neurology, Universitätsspital BaselRecrute dans ce centre
- Bern, SuisseDept, of Neurology, Inselspital, University of BernRecrute dans ce centre
Au total, dans le monde, les 3 centres listés au registre recrutent.
Statut par centre selon le registre ClinicalTrials.gov (dernière mise à jour publiée : 13 décembre 2024).
Ce statut peut avoir changé et ne dit rien de votre éligibilité : avant toute démarche, vérifiez avec votre oncologue ou le centre.
Autres identifiants
- 2021-01797 · autre identifiant
Voir aussi
Autres versions
Ces résultats sont indicatifs et ne remplacent pas un avis médical — à discuter avec votre médecin.