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Effect of prior informed consent on the treatment of patients with acute ischemic stroke - a prospective randomized controlled trial that advances communication to an ambulance

Effect of prior informed consent on the treatment of patients with acute ischemic stroke - a prospective randomized controlled trial that advances communication to an ambulance

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018878
Enrollment
Unknown
Registered
2018-10-14
Start date
2018-10-11
Completion date
Unknown
Last updated
2018-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute ischemic stroke

Interventions

Group 1:Start communicating ahead of time
Group 2:none

Sponsors

Jingjiang People'sHospital, Shaoxing Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The ambulance will be called within 6 hours after the onset of illness, and will be taken by the ambulance of the hospital and escorted to the acute ischemic stroke patients in the emergency department of the hospital.

Exclusion criteria

Exclusion criteria: Patients who were not confirmed to have a non-acute ischemic stroke or who were not indicated for intravenous thrombo/intravascular treatment after admission.

Design outcomes

Primary

MeasureTime frame
NIHSS score at discharge;MRs score at 3 months;;—

Secondary

MeasureTime frame
Call for help - departure time;Departure time - return time (transportation kilometers);Emergency - intravenous thrombolysis time / femoral artery puncture time;;Incidence - intravenous thrombolysis time / femoral artery puncture time;personal information;—

Countries

China

Contacts

Public ContactDing Yun-Long

Jingjiang People's Hospital, Shaoxing Second Hospital

dingyunlong66@sina.com+86 15861035745

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026