Trials / Terminated
TerminatedNCT00795587
Comparison of 2 Doses of Mannitol on Post Traumatic Intracranial Hypertension and Cerebral Monitoring
Compared Effects of 2 Doses of Mannitol on Post Traumatic Intracranial Hypertension
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 3 (actual)
- Sponsor
- University Hospital, Grenoble · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Will an increase of the dose of mannitol improve the effects on neuromonitoring in patients suffering intracranial hypertension following traumatic brain injury?
Detailed description
traumatic brain injury intracranial hypertension 0,4 g/ kg vs 0,8 g/ kg (randomized) on 20 minutes monitoring: ICP, transcranial doppler, brain pO2, MAP, HR, diuresis, biology duration: 2 hours
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | variation of mannitol dose | in case of intracranial hypertension up to 20 mmHg lasting more than 10 minutes and without nociceptive stimulation or systemic instability: injection of either 0.4 g/ kg or 0.8 g/ kg of mannitol 20% (randomized) on 20 minutes, with monitoring of neurologic, systemic and biologic datas during 120 minutes |
Timeline
- Start date
- 2008-10-01
- Primary completion
- 2011-08-01
- Completion
- 2011-08-01
- First posted
- 2008-11-21
- Last updated
- 2012-11-08
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT00795587. Inclusion in this directory is not an endorsement.