Risk of Recurrent CeAD After Pregnancy

Part of paid clinical trials in Salt Lake City, Utah.

Sponsor
University Hospital, Basel, Switzerland
Study ID
NCT06258109
Status
Recruiting
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Conditions

  • Cervical Artery Dissection
  • Pregnancy Complications

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

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.

Key Dates

Start date
Jan 1, 2023
Status verified
Dec 2024
Primary completion
Dec 1, 2024
Completion
Jul 1, 2025

Study Design

Enrollment
1,000 participants (estimated)

Arms

  • Arm: Women with pregnancy after index CeAD
    Women who became pregnant at least once after first index CeAD
  • Arm: Women without pregnancy after index CeAD
    Women who did not became pregnant after first index CeAD

Primary Outcome Measure

Number of participants with composite outcome measure - recurrent CeAD, ischemic stroke, hemorrhagic stroke and/or death [ Time Frame: From date of first CeAD until date of latest follow-up assessed up to 35 years ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
University of UtahSalt Lake CityUtah84112-
University of VirginiaCharlottesvilleVirginia22908-

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