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Clevidipine for the Antihypertensive Treatment of Acute Intracerebral Hemorrhage
NCT06402968 · View on ClinicalTrials.gov ↗
Study Summary
The aim is to compare the rate of hypertensive subjects with ICH who reach SBP target with stability within 60 minutes of enrollment, among patients treated with IV clevidipine with those treated with alternate IV antihypertensive regimen.
Conditions Studied
Interventions
- DRUG Clevidipine Injection
- DRUG Alternate IV Antihypertensive Regimen
Study Locations (9)
Texas
- UT Southwestern Medical Center — Dallas
- University of Texas Health Science Center San Antonio — San Antonio
California
- Antelope Valley Medical Center — Lancaster
Florida
- Cleveland Clinic Martin North Hospital — Stuart
Georgia
- Augusta University-Neuroscience Center — Augusta
Michigan
- University of Michigan Health-West — Wyoming
Missouri
- University of Missouri — Columbia
New York
- Icahn School of Medicine at Mount Sinai — New York
Ohio
- Cleveland Clinic Foundation — Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,000 participants |
| Start Date | 2024-06-01 |
| Est. Completion | 2028-07-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06402968
The ClinicalTrials.gov registry entry for NCT06402968 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zeenat Qureshi Stroke Institute, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Hypertension appearing as the primary indexed condition, and to 2 interventions — of which Clevidipine Injection is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06402968 reports 9 study locations spanning 8 distinct geographic areas — top geographies include Texas, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06402968 about?
NCT06402968 is a clinical study titled "Clevidipine for the Antihypertensive Treatment of Acute Intracerebral Hemorrhage". The aim is to compare the rate of hypertensive subjects with ICH who reach SBP target with stability within 60 minutes of enrollment, among patients treated with IV clevidipine with those treated with alternate IV antihypertensive regimen.
What is the current status of trial NCT06402968?
This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2024-06-01. Estimated completion is 2028-07-30.
What conditions does trial NCT06402968 study?
This clinical trial studies the following conditions: Hypertension, Stroke, Intracerebral Hemorrhage. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06402968?
The interventions under investigation include: Clevidipine Injection (DRUG), Alternate IV Antihypertensive Regimen (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06402968?
This trial is sponsored by Zeenat Qureshi Stroke Institute, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06402968 being conducted?
This trial has 9 study locations across California, Florida, Georgia, Michigan, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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