Actively Recruiting
Beta-1 Adrenergic Inhibition to Reduce Cardiac Injury and Inflammation After Subarachnoid Hemorrhage (BADCATS)
Led by Madeleine Puissant · Updated on 2024-11-26
20
Participants Needed
1
Research Sites
257 weeks
Total Duration
On this page
Sponsors
M
Madeleine Puissant
Lead Sponsor
M
MaineHealth
Collaborating Sponsor
AI-Summary
What this Trial Is About
To determine the effect of early metoprolol administration after non-traumatic subarachnoid hemorrhage (SAH).
CONDITIONS
Official Title
Beta-1 Adrenergic Inhibition to Reduce Cardiac Injury and Inflammation After Subarachnoid Hemorrhage (BADCATS)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Older than 18 years of age
- Neuro-imaging confirmed non-traumatic subarachnoid hemorrhage
You will not qualify if you...
- Traumatic cause of subarachnoid hemorrhage such as fall, motor vehicle accident, or other blunt trauma
- Other types of intracranial bleeding including intracerebral hemorrhage, subdural hemorrhage, or epidural hemorrhage
- Pregnancy
- Unstable vital signs not suitable for beta-1 adrenergic receptor inhibitor treatment including systolic blood pressure below 80 mmHg not stabilized by medications, heart rate below 50 beats per minute with low blood pressure, or need for vasopressor agents due to hypotension
- Any other vital sign concerns as determined by the treatment team
- History of severe heart failure (Stage C or D or NYHA Class III or IV)
- Unwillingness or inability of patient or legal representative to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
MaineHealth
Portland, Maine, United States, 04012
Actively Recruiting
Research Team
M
Madeleine Puissant, MD, PhD
CONTACT
C
Christine Lord
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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