Intracranial aneurysm, abdominal aortic aneurysm brainaneurysm, aorta aneurysm
Conditions
Interventions
Abdominal ultrasound of the aorta as described 
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a participant must meet all of the following criteria:Patient is a study subject of the trial: Study on Prognosis of Acutely RupTured Aneurysms (SPARTA)Written informed consent By being a study subject of the SPARTA trial, the following criteria are applicable:Confirmed diagnosis of SAH on CT-scan or lumbar puncture (in the presence of a negative CT-scan).IA related SAH as confirmed with radiological imaging.Age 18 years or olderWritten informed consent for the SPARTA-trial
Exclusion criteria
Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study:Patient is not a study subject of the SPARTA trialPatient has Loeys-Dietz-, Marfan- or Ehlers-Danlos syndrome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome, which will be investigated in the here above described study population, is the number of abdominal aortic aneurysms detected on abdominal ultrasound. | — |
Secondary
| Measure | Time frame |
|---|---|
| Risk factors for having an abdominal aortic aneurysm, while being a patient who had aSAH | — |
Countries
Netherlands
Contacts
Public ContactAL Hamming
Leids Universitair Medisch Centrum
Outcome results
None listed