Overview
High Dose Hyperoncotic Serum Albumin for the Treatment of the Acute Phase of Severe Head Injury
Status:
Unknown status
Unknown status
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
Experimentally high dose of hyperoncotic human serum albumin improve neurological recovery after head injury reduce cerebral edema and normalize apparent diffusion coefficient of water after ischemia reperfusion. The main hypothesis is that early administration of hyperoncotic serum albumin is able to reduce intracranial pressure for several days after severe head injury and thus reduce mortality and morbidity.Phase:
Phase 2/Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University Hospital, Angers
Criteria
Inclusion Criteria:- severe head injury (GCS < 9) Next of kin informed consent
Exclusion Criteria:
- Cranio cerebral wound Pregnancy Hypoxemia (PaO2/FiO2< 300 mmHg) Blood loss > 1/2 blood
mass Renal or cardiac failure,uncontrolled hypertension Head injury dating from more
than 24 hours at the time of inclusion