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Deferoxamine in Aneurysmal Subarachnoid Hemorrhage trial

Deferoxamine in Aneurysmal Subarachnoid Hemorrhage trial - DASH

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON52890
Enrollment
40
Registered
2019-04-10
Start date
2022-12-02
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

cerebral vasospasm Delayed cerebral ischemia

Interventions

Deferoxamine for 3 consecutive days. Patients will receive an intravenous dose of 32 mg/kg/day.

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • 18-85 years old inclusive, • Subarachnoid hemorrhage diagnosed by CT on admission, • No history of possible traumatic origin of subarachnoid hemorrhage, • Eligible for inclusion within 72 hours of subarachnoid hemorrhage, • Saccular intracranial aneurysm proven by cerebral angiography or CTA, • Surgical or endovascular obliteration is successfully performed, • Able to obtain written informed consent from patient or surrogate, • Patients in good clinical grade (WFNS 1-3) (GCS 13-15) at time of inclusion.

Exclusion criteria

Exclusion criteria: • Pregnancy, as confirmed by routine urine test on admission, • Abnormal renal function at time of inclusion (eGFR 35 U/L and ALT > 45 U/L.) • History of liver disease or active liver or renal disease, • Patients with low ferritine (30), o SpO2 30) o Acidosis (pH

Design outcomes

Primary

MeasureTime frame
Primary endpoint is the occurrence of DCI

Secondary

MeasureTime frame
Secundary endpoint is the total number of patients with drug related adverse events.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)