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Clinical Effectiveness Study of a Full-Process Orthopedic AI Agent

Clinical Effectiveness Study of a Full-Process Orthopedic AI Agent

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124363
Enrollment
Unknown
Registered
2026-05-11
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Various types of fractures

Interventions

Control Group:Standard Clinical Care
Experimental Group:Full-process Orthopedic AI Agent Assisted Diagnosis and Treatment

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients hospitalized in the department of orthopedics at our hospital during the study period; 2. Age >= 18 years. 3. The patient and their family members voluntarily participate in this study and sign the written informed consent form. 4. Willing to comply with the study procedures and cooperate with the implementation of the entire study process.

Exclusion criteria

Exclusion criteria: 1. Patients with severe mental illness or cognitive impairment who are unable to understand the study content or cooperate with the study. 2. Patients unsuitable for participation due to legal or ethical reasons (e.g., pregnant or lactating women). 3. Other conditions deemed unsuitable for participation by the investigator, such as the presence of severe comorbidities that may interfere with outcome assessment, or conflicts arising from participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Diagnostic Accuracy;Hospital Workflow Efficiency (Average Length of Stay, LOS);Hospital Unit Time Revenue (Average revenue per bed-day and total revenue growth rate);

Secondary

MeasureTime frame
Hospitalization Costs (Average Total Cost per Patient);Physician Efficiency and Workload (e.g., Average Documentation Time);Patient Satisfaction (Doctor-Patient Communication Harmony);Clinical Prognosis and Safety (Perioperative Complication Rate, 30-day Readmission Rate, etc.);

Countries

China

Contacts

Public ContactLei Wang

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

ray_wangs@hotmail.com+86 21 64370045

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026