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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00248690
Other study ID # 2005-SAHD
Secondary ID S-05184
Status Completed
Phase N/A
First received October 25, 2005
Last updated January 17, 2011
Start date November 2005
Est. completion date June 2009

Study information

Verified date January 2008
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Medicines AgencyNorway: The Data InspectorateNorway: Directorate of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether treatment guided also by ICP mean wave amplitude improves outcome compared to international standard care in patients with SAH.


Description:

In this study SAH-patients are randomized to treatment based on international standard care (ICP/CPP guided therapy) or intracranial compliance (ICP mean wave amplitude) guided therapy in addition to ICP/CPP guided therapy. Main outcome variables are survival and neurological outcome after 3 and 12 months.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date June 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subarachnoid hemorrhage, acute

- Intracerebral pressure monitoring device inserted

Exclusion criteria:

- No intracranial pressure monitoring

- Age < 18 years

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)


Intervention

Device:
ICP mean wave amplitude
Appropriate measures when ICP mean wave amplitude is to high, e.g. CSF drainage

Locations

Country Name City State
Norway Rikshospitalet University Hospital Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary All cause mortality and neurological outcome 3 and 12 months No
Secondary Length of stay (ICU, hospital); complications; effect of treatment modalities on mean ICP, CPP, ICP mean wave amplitude. Hospital stay Yes
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