Risk of Recurrent CeAD After Pregnancy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity Hospital, Basel, Switzerland
About this trial
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.
Eligibility criteria
Qualifiers
female
prior symptomatic cervical artery dissection (= index CeAD)
at least one long-term follow-up visit (at least 6 months after the initial event)
recurrent dissection
Disqualifiers
Male patients
Age <18 years
No long-term follow-up available or long-term follow-up < 6 months after initial event
No data on pregnancy after initial event available
Trial design
Treatments tested in this trial
- Not listed
Trial groups
1,000 Participants
are grouped into 2 trial groupsLocations
12Argentina
Stroke Unit Sanatorio AllendeX5000BFB, Córdoba Argentina
Austria
Department of Neurology, Medical University of Innsbruck6020, InnsbruckTyrol, Austria
Finland
Helsinki University Central Hospital Helsinki Finland
Germany
Charité Universitätsmedizin, Centrum für Schlaganfallforschung10117, Berlin Germany
Sponsors and collaborators
University Hospital, Basel, Switzerland
Lead sponsor
Source ClinicalTrials.gov