NCT07018167Active, not recruitingNot Applicable
Impact of Door-to-Needle Time on Stroke Outcomes at Gonesse Hospital
Centre Hospitalier de Gonesse1 site in 1 country61 target enrollmentStarted: May 1, 2025Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 61
- Locations
- 1
- Primary Endpoint
- Time (in minutes) from hospital arrival to thrombolysis (Door-to-Needle Time).
Study Overview
Brief Summary
This study looks at how quickly stroke patients receive treatment after arriving at Gonesse Hospital and whether this affects their recovery. Researchers will measure the time between a patient's arrival and the start of clot-busting treatment (called Door-to-Needle Time), as well as the time from symptom onset to hospital arrival (Home-Time). The goal is to see if treatment delays impact recovery, and to find ways to improve stroke care in the hospital.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Retrospective
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients aged 18 years or older
- •Confirmed diagnosis of acute ischemic stroke on imaging
- •Initial acute stroke care provided at Gonesse Hospital during the study period (3 months)
- •Intravenous thrombolysis (r-tPA) initiated at the hospital
- •Availability of clinical and timing data to calculate Door-to-Needle Time (DNT)
Exclusion Criteria
- •Patients with hemorrhagic stroke or subarachnoid hemorrhage (SAH)
- •Thrombolysis initiated before hospital arrival
- •Missing, incomplete, or unusable timing data for DNT calculation
Outcomes
Primary Outcomes
Time (in minutes) from hospital arrival to thrombolysis (Door-to-Needle Time).
Time Frame: 3 months
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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