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

Centre Hospitalier de Gonesse

Status: Active, not recruiting

Conditions: Cerebral Infarction; Ischemic Attack, Transient; Stroke; Treatment Outcome; Thrombolytic Therapy

Study type: Observational

Funder types: Other

Identifiers

NCT07018167

0107_NEUROLOGIE

Details and patient eligibility

About

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.

Enrollment: 61 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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