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Acetazolamide as a treatment after hemorrhagic stroke

Acetazolamide in Aneurysmal Subarachnoid Hemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23709
Enrollment
40
Registered
2017-03-02
Start date
2017-05-01
Completion date
Unknown
Last updated
2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

aneurysmal subarachnoid hemorrhage

Interventions

In the intervention group, subjects will receive acetazolamide intravenously as well as treatment as usual. The dosage of acetazolamide will be similar to the average dosage used for the treatment of

Sponsors

University Medical Center Utrecht
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ≥18 years old Aneurysm confirmed by the presence of subarachnoid blood by computed tomography (CT) or lumbar puncture and by visualization of the aneurysm on either CT angiography, MR angiography or digital subtraction angiography Hospital arrival ≤72 hours of ictus Eligible for aneurysm coiling

Exclusion criteria

Exclusion criteria: Intensive care (IC) required for >72 hours after ictus (i.e., during inclusion window) Perimesencephalic bleeding Traumatic SAH Severe liver dysfunction or severe renal dysfunction Allergic reaction for sulfomides Any contraindication for MR imaging (e.g. metal objects within or around the body) Pregnancy or women who are breastfeeding Addison’s disease Phenytoin use

Design outcomes

Primary

MeasureTime frame
Cerebral perfusion (arterial spin labeling (ASL) MRI) on day 7±2 after ictus.

Secondary

MeasureTime frame
Cerebral perfusion (arterial spin labeling (ASL) MRI) on day 12±2 after ictus. Serious adverse events (SAEs) and serious unexpected serious adverse reactions (SUSARs) until 10 weeks after ictus. The occurrence of DCI. DCI will be defined as either “clinical deterioration or cerebral infarction due to delayed cerebral ischemia”.

Contacts

Public ContactLisa van der Kleij

Postbus 85500

L.vanderKleij-4@umcutrecht.nl088 7550643

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)