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Study identifier: NCT06258109 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Risk of Recurrent CeAD After Pregnancy

Condition: Cervical Artery Dissection · Pregnancy Complications  ·  Sponsor: University Hospital, Basel, Switzerland

PhaseN/A
Planned participants1000
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Primary objective: To determine whether pregnancy increases the risk of recurrent CeAD and delayed stroke in women with prior CeAD based on long-term data. Methods: Multicentric, observational case-control study based on pooled individual patient data from several stroke centers. Primary endpoint: Primary composite outcome measure includes the following outcomes: (i) occurrence of recurrent CeAD, (ii) occurrence of ischemic or hemorrhagic stroke, (iii) death.

This description comes directly from the study's public registry record.

Talk to the study team

Stefan T Engelter, MD  ·  +41 61 326 41 05  ·  stefan.engelter@felixplatter.ch

Sandro K Fischer  ·  +41 61 328 47 84  ·  sandrokevin.fischer@usb.ch

Always discuss trial participation with your own doctor first.

Locations (12)

University of UtahSalt Lake City, Utah, United StatesRecruiting
University of VirginiaCharlottesville, Virginia, United StatesRecruiting
Stroke Unit Sanatorio AllendeCórdoba, ArgentinaRecruiting
Department of Neurology, Medical University of InnsbruckInnsbruck, Tyrol, AustriaRecruiting
Helsinki University Central HospitalHelsinki, FinlandRecruiting
Charité Universitätsmedizin, Centrum für SchlaganfallforschungBerlin, GermanyRecruiting
Neurologische Klinik und Poliklinik, LMU Klinikum Campus GroßhadernMunich, GermanyRecruiting
Hadassah-Hebrew University Medical CenterJerusalem, IsraelRecruiting
Neurology Clinic, University of BresciaBrescia, ItalyRecruiting
Stroke Clinic, National Institute of Neurology and Neurosurgery Manuel Velasco SuárezMexico City, MexicoRecruiting
University Hospital Basel, Stroke CenterBasel, SwitzerlandRecruiting
University Hospital Zurich, Stroke CenterZurich, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT06258109