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Artificial Intelligence in Emergency Medicine

Artificial Intelligence in Emergency Medicine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125287
Enrollment
Unknown
Registered
2026-05-25
Start date
2025-04-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Advanced Cancer

Interventions

ChatGPT-4.0 group:AI-generated treatment recommendations: All participants received a personalized resuscitation recommendation document generated based on their own clinical information (including de
Deepseek group:AI-generated treatment recommendations: All participants received a personalized resuscitation recommendation document generated based on their own clinical information (including demo
Grok group:AI-generated treatment recommendations: All participants received a personalized resuscitation recommendation document generated based on their own clinical information (including demograph

Sponsors

Cancer Hospital Of Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patient characteristics Age: >= 18 years old and = 13 points (basic consciousness is clear and can cooperate with the collection of medical history). 2. Medical conditions Relative stability of vital signs (systolic blood pressure >= 90 mmHg, respiratory rate = 92%); Complete basic examinations (at least including blood routine, electrocardiogram, and one of the chest/abdominal imaging tests). 3. Process compliance Case information can be fully exported from the electronic medical record system (including timestamp records); Doctor's operations are completed throughout the process on the standardized research platform (traceable operation logs).

Exclusion criteria

Exclusion criteria: 1.Clinical Contraindications Critically ill patients requiring immediate resuscitation (e.g., cardiac arrest, severe trauma, shock); Pregnant or breastfeeding women (due to specific treatment limitations); Patients with known end-stage disease (life expectancy < 72 hours). 2.Information Integrity Constraints Language or cognitive impairments preventing reliable history taking; Missing critical information in pre-hospital emergency records (e.g., symptom onset time). 3.Study Interference Factors Concurrent participation in other interventional clinical trials; Special cases involving medical disputes or forensic identification.

Design outcomes

Primary

MeasureTime frame
Diagnostic consistency;

Secondary

MeasureTime frame
Comparison results among models;

Countries

China

Contacts

Public ContactLifeng Xiao

Cancer Hospital Of Shantou University Medical College

xiaolifeng05@163.com+86 754 8859 9551

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026