Purpose

The DOME study is a clinical trial exploring a new treatment approach for patients who suffered a severe brain bleed due to an aneurysm.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 18 years or older - CT confirmed aSAH with an angiographically detected aneurysm - World Federation of Neurological Sciences (WFNS) aSAH grade 3-5 aneurysm - LAR available and gives consent within 72 hours after the onset of aSAH (or last known normal

Exclusion Criteria

  • Patients whose aneurysm judged appropriate for balloon-assisted coiling - Patients whose aneurysm is bleeding from the "neck" - Patients who are clinically judged to suffer imminent death within 24 hours. - Pregnancy or positive urine pregnancy test

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Recruiting Locations

University of Louisville Hospital
Louisville, Kentucky 40202
Contact:
Mechelle Kaufman, BSN
502-852-1513
mechelle.kaufman@louisville.edu

More Details

Status
Recruiting
Sponsor
University of Louisville

Study Contact

Detailed Description

To prospectively capture data of patients treated with the guideline-recommended, standard-of-care dome-protection approach. The data will be used to determine: - (Primary) Incidence of aneurysm re-rupture by 90 days, censored at the time of definitive aneurysm treatment or death, detected on a surveillance head CT or one obtained after a neurological decline. - (Secondary) Measure functional status of patients around 90 days (+/- 14 days) - (Secondary) Measure success of dome protection as determined by angiographic criteria and procedural complications DOME protection is a treatment approach for patients who suffered a severe brain bleed due to an aneurysm. Instead of performing immediate, extensive surgery, this study investigates a minimally invasive procedure called "dome protection", which involves placing tiny coils to patch the most fragile part of the aneurysm. This method aims to prevent re-bleeding and allow the patient to stabilize before undergoing full aneurysm repair. The findings could lead to improved health outcomes in patients with aneurysmal subarachnoid hemorrhage by reducing procedure-related risks.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.