Subarachnoid Hemorrhage Clinical Trial
| Verified date | June 2007 |
| Source | University of Illinois at Chicago |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Observational |
The purpose of this research is to explore ways to improve and simplify control of blood pressure in patients with SAH or ICH. This research will be done by comparing tow different medications that are routinely used to help control blood pressure. None of the medications used in this study nor any procedures performed are experimental.
| Status | Completed |
| Enrollment | 163 |
| Est. completion date | February 2007 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 70 Years |
| Eligibility |
Inclusion Criteria: - 18-70 years old (inclusive) - Admission to NSICU with a diagnosis of SAH or ICH Exclusion Criteria: - Patients who are admitted >48 hours after SAH or ICH - Readmission or second SAH - Readmission or second ICH - Large (immediately life threatening) associated intraparenchymal or intraventricular hemorrhage - Women who are pregnant |
Observational Model: Defined Population, Time Perspective: Longitudinal
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Illinois at Chicago, UIC | Chicago | Illinois |
| Lead Sponsor | Collaborator |
|---|---|
| University of Illinois at Chicago |
United States,
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