IV Double and Triple Concentrated Nicardipine for Stroke and ICH
Part of paid clinical trials in Peoria, Illinois.
- Sponsor
- OSF Healthcare System
- Study ID
- NCT00325793
- Phase
- PHASE4
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nicardipine — DRUG
Study Details
Hypertension (high blood pressure) can often cause neurological worsening in patients with stroke, intracerebral hemorrhage and subarachnoid hemorrhage. Intravenous infusion of nicardipine (Cardene) for control of hypertension is FDA approved. The disadvantage of Nicardipine IV drip is the relative large volume of fluid needed (up to 150 cc/hr). The purpose of this study is to evaluate safety and efficacy of double or triple concentrated peripheral intravenous (IV) Nicardipine.
Key Dates
- Start date
- Jan 31, 2004
- Status verified
- May 2006
Study Design
- Enrollment
- 50 participants
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Primary Outcome Measure
• Demonstrate the feasibility and safety of double and triple concentrated peripheral intravenous Nicardipine for patients in the Neuroscience Critical Care Unit.
Central Contacts
- David Wang, DO309-624-9500
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| OSF Stroke Center | Peoria | Illinois | 61637 | David Wang, DO (PRINCIPAL_INVESTIGATOR) |
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