NCT06258109Recruiting
Risk of Recurrent CeAD After Pregnancy
Long-term Risk of Recurrent Cervical Artery Dissection After Pregnancy (LONG-RECAP Study)
Source: ClinicalTrials.gov · Last updated 13 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 1000 (estimated)
- First submitted
- 11 Jan 2024
- Start date
- 1 Jan 2023
- Primary completion date
- 1 Dec 2024
- Lead sponsor
- University Hospital, Basel, Switzerland
- Diseases
- Stroke
- NCT number
- NCT06258109
What you commit to
- Study type: Observational
- Planned participants: 1000
- From 1 Jan 2023 to the primary completion date, 1 Dec 2024
- 12 sites in 9 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Age \<18 years
Other
- Male patients
- No long-term follow-up available or long-term follow-up \< 6 months after initial event
- No data on pregnancy after initial event available
Who the study is looking for
- female
- prior symptomatic cervical artery dissection (= index CeAD)
- at least one long-term follow-up visit (at least 6 months after the initial event)
- with information available on outcome events:
- recurrent dissection
- ischemic stroke
- hemorrhagic stroke
- functional outcome assessed by mRS score
- with data on pregnancy after the initial event
- at least 18 years old at the initial event
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (12)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Stroke Unit Sanatorio Allende Coordinator of this site? Confirm its status | Córdoba | Argentina | Recruiting |
| Department of Neurology, Medical University of Innsbruck Coordinator of this site? Confirm its status | Innsbruck | Austria | Recruiting |
| University Hospital Basel, Stroke Center Coordinator of this site? Confirm its status | Basel | Switzerland | Recruiting |
| University Hospital Zurich, Stroke Center Coordinator of this site? Confirm its status | Zurich | Switzerland | Recruiting |
| Charité Universitätsmedizin, Centrum für Schlaganfallforschung Coordinator of this site? Confirm its status | Berlin | Germany | Recruiting |
| Neurologische Klinik und Poliklinik, LMU Klinikum Campus Großhadern Coordinator of this site? Confirm its status | Munich | Germany | Recruiting |
| Helsinki University Central Hospital Coordinator of this site? Confirm its status | Helsinki | Finland | Recruiting |
| Hadassah Hebrew University Medical Center Coordinator of this site? Confirm its status | Jerusalem | Israel | Recruiting |
| Neurology Clinic, University of Brescia Coordinator of this site? Confirm its status | Brescia | Italy | Recruiting |
| Stroke Clinic, National Institute of Neurology and Neurosurgery Manuel Velasco Suárez Coordinator of this site? Confirm its status | Mexico City | Mexico | Recruiting |
| University of Virginia Coordinator of this site? Confirm its status | Charlottesville | United States | Recruiting |
| University of Utah Coordinator of this site? Confirm its status | Salt Lake City | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.