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A Clinical Study Protocol to Improve the Implementation Rate of Pre-hospital Ambulance Guidelines for Acute Cardiovascular Disease Based on the Pre-hospital Emergency Information System (IEMSCVD)

A Clinical Study Protocol to Improve the Implementation Rate of Pre-hospital Ambulance Guidelines for Acute Cardiovascular Disease Based on the Pre-hospital Emergency Information System (IEMSCVD)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088833
Enrollment
Unknown
Registered
2024-08-27
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

Acute cardiovascular disease

Interventions

Traditional implementation strategy group(control group):Using traditional implementation strategies to execute the clinical pathway of pre hospital emergency care, including: 1) multidisciplinary com
2) Education and training on clinical pathways
3) Regularly organize seminars to evaluate implementation effectiveness and provide feedback(phase 1 and phase 2)
IEMSCVD implementation strategy group(intervention group):Including traditional implementation strategies, as well as implementation strategies equipped with intelligent software: 1) clinical decision
2) Online consultation
3) Sharing of diagnosis and treatment data in front and inside the hospital premises(phase 1 and phase 2)

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The patient calling 120 has a circulatory system emergency and meets the initial symptoms of acute cardiovascular disease. The specific initial symptoms include chest pain/tightness, waist/back pain, difficulty breathing, palpitations, dizziness/vertigo, headache, hemoptysis, cough, syncope, coma, fainting, etc.

Exclusion criteria

Exclusion criteria: 1:   Due to other basic diseases, patient are in the terminal stage of survival 2:   Patients who call 120 due to trauma, poisoning/physical and chemical injuries, obstetrics and gynecology emergency, digestive system emergency, facial emergency, infectious diseases, mental illnesses, simple transportation, etc 3:   Without informed consent

Design outcomes

Primary

MeasureTime frame
90 day all-cause mortality rate;

Secondary

MeasureTime frame
6-hour discharge rate ;Process indicators;Adoption;Implementation;Maintenance;90 day readmission rate;In-hospital mortality rate;Reach;Effectiveness;

Countries

China

Contacts

Public ContactJiang Hong

Renmin Hospital of Wuhan University

wlang81@126.com+86 159 2716 2528

Outcome results

None listed

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