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Platelet transfusion in brain haemorrhage

Platelet transfusion in cerebral haemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28517
Enrollment
190
Registered
2008-04-29
Start date
2008-06-01
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Intracerebraal hematoom CVA Beroerte Trombocyten transfusie Intracerebral haemorrhage Stroke Platelet transfusion Anti-platelet therapy

Interventions

- 95 patients receive platelet transfusion as soon as possible within 6 hours after onset - 95 patients receive standard care Platelet transfusion consists of a single gift of 5 or 10 donor units de

Sponsors

AMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age > 18 years 2. Non-traumatic, primary, supratentorial ICH 3. Haematoma volume > 150 cc 4. GCS score 8-15 5. Anti-platelet therapy for at least the previous 7 days 6. Transfusion can be started < 6 hrs after onset 7. Transfusion can be started < 1,5 hrs after CT 8. mRankin scale score before ICH 0 or 1 9. Informed consent obtained

Exclusion criteria

Exclusion criteria: 1. Bleeding pattern on CT suggestive of AVM or aneurysm 2. Haematoma evacuation planned < 24 hrs 3. Intraventricular haemorrhage (sedimentation in posterior horns is allowed) 4. Previous adverse reaction to platelet transfusion 5. Known use of vitamine K antagonists 6. Known thrombocytopenia < 100 x 109/l 7. History of coagulopathy 8. Previously legally incompetent adults prior to stroke 9. Death appears imminent

Design outcomes

Primary

MeasureTime frame
Poor outcome defined as a modified Rankin Scale (mRS) score 4-6 after 3 months.

Secondary

MeasureTime frame
- Haematoma growth on CT in the first 24 hours - Complications of platelet transfusion - Whether the CTA "spot sign" can predict primary outcome - Whether the CTA "spot sign" can predict haematoma enlargement on CT - Survival rate and level of physical disability at three months - Functional health at three months using the full ordinal scoring range of the mRS - Costs

Contacts

Public ContactIrem Baharoglu

Department of Neurology Academic Medical Center University of Amsterdam

m.i.baharoglu@amc.uva.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)