Study on Prognosis of Acutely Ruptured Intracranial Aneurysms
Recruiting
Observational Study
Aneurysmal Subarachnoid Hemorrhage
Endovascular Procedures
Craniotomy
Patient Outcome Assessment
Treatment Outcome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 880 (estimated)
- Sponsor
- Haaglanden Medical Centre · Other
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About This Trial
The SPARTA study is a prospective multicenter observational trial in the Netherlands with the aim of identifying the best clinical care in patients with aneurysmal subarachnoidal haemorrhage. Differences in outcome between surgical treatment and endovascular treatment will be explored. Furthermore, cost effectiveness and radiological prognostic factors will be examined.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Confirmed diagnosis of subarachnoid haemorrhage on CT-scan or lumbar puncture (in the presence of a negative CT-scan)
* Intracranial aneurysm proven within 6 months to be the cause of subarachnoid haemorrhage
* Age 18 years or over at presentation.
* Written informed consent
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Contacts