Impact of Door-to-Needle Time on Stroke Outcomes at Gonesse Hospital

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

61 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-05-01

Study Completion Date

2025-09-01

Brief Summary

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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.

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Detailed Description

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Conditions

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Stroke Ischemic Attack, Transient Cerebral Infarction Thrombolytic Therapy Treatment Outcome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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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

Eligible Sex

ALL

Accepts Healthy Volunteers

No