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High Dose Hyperoncotic Serum Albumin for the Treatment of the Acute Phase of Severe Head Injury

Phase 2
Conditions
Severe Head Injury
Registration Number
NCT00152685
Lead Sponsor
University Hospital, Angers
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Reduction of the daily median value of intracranial pressure
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Neurosurgical intensive care. CHU de Nancy

🇫🇷

Nancy, France

Surgical intensive care. CHU

🇫🇷

Angers, Cedex 9, France

Neurosurgical intensive care. CHU Le Kremlin Bicêtre

🇫🇷

Le Kremlin Bicêtre, France

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