Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseobservationalRules rewrite
Not a traditional drug phase: Standard of care (no study intervention) for Stroke
Stroke is a leading cause of death and adult disability. Stroke care is still limited by fragmented care pathways, non-standardised diagnostic work-up and follow-up, and local, non-interoperable data systems across the pre-hospital, in-hospital and post-hospital settings.
This is an observational study. You are not assigned a new experimental drug. Researchers measure what already happens in your care or in daily life.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
This listing is observational (StudyType). The registry does not assign a new experimental drug as the study intervention.
They plan to enroll about 10,000 people at 7 sites. Taking part typically means study visits and measurements plus check-ins.
Official title (unrewritten)
Unleashing a CoMprehensive, Holistic and Patient Centric Stroke Management for a Better, Rapid, AdvancEd and PersonaLised Stroke Diagnosis, TreAtment and Outcome Prediction (UMBRELLA) - Prospective Clinical Study
Interventions: Standard of care (no study intervention)
Primary outcome (registry wording): Area Under the Curve (AUC) of the Pre-hospital AI Model for Detection of Large Vessel Occlusion (LVO) Stroke (WP2)
Who it is for (from inclusion criteria)
Ages 18 Years to any
Age 18 years or older
Clinical suspicion of acute stroke (including TIA)
Additional who can join by sub-study:
WP2 and WP3: suspected stroke according to ambulance personnel or confirmed LVO stroke, AND symptom onset (or last seen well, if unwitnessed) less than 24 hours earlier
WP4: intracerebral hemorrhage, regardless of sex, risk factors or etiology
WP5: NIHSS below 7 AND premorbid mRS below 4
WP6: acute ischemic stroke, with or without atrial fibrillation
Who the registry excludes
People the protocol lists as excluded — the study team must confirm.
We will investigate the clinical manifestations and molecular genetic defects of heritable urologic malignant disorders. Families with urologic malignancy with known or suspected genetic basis will be enrolled.
This protocol will evaluate patients with systemic lupus erythematosus (SLE) and their relatives to learn more about how the disease develops and changes over time. It will also study genetic factors that make a person susceptible to SLE.
This study is designed to explore the genetics and pathophysiology of diseases presenting with intermittent fever, including familial Mediterranean fever, TRAPS, hyper-IgD syndrome, and related diseases. The following individuals may be eligible for this natural history study: 1) patients with known or suspected familial Mediterranean fever, TRAPS, hyper-IgD syndrome or related disorders; 2) relatives of these patients; 3) healthy, normal volunteers 7 years of age or older.
The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT07924371?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT07924371?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.