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Research on the Clinical and Social Value of Intelligent Safe Medical Transport Equipment for Intrahospital Transfer of Critically Ill Patients

Research on the Clinical and Social Value of Intelligent Safe Medical Transport Equipment for Intrahospital Transfer of Critically Ill Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102580
Enrollment
Unknown
Registered
2025-05-16
Start date
2025-02-21
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

None

Interventions

Intelligent transport group:None
Control group:None
Experimental group(medical staff):None
Control group(medical staff):None

Sponsors

Xuanwu Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients: 1. Consent to participate in the study. Patients or their legal representatives have signed an informed consent form and agreed to participate in all procedures of the study; 2. Critically ill patients; 3. Perioperative patients; 4. Patients with limited mobility. Health care workers: 1. Agree to participate in the study, have signed the informed consent form, and agree to participate in all processes of the study; 2. Have obtained the professional qualification certificate; 3. Medical staff working in emergency department, operating room and ICU. 4. Have worked in the hospital for at least one year.

Exclusion criteria

Exclusion criteria: Patients: 1. Refusal to sign the informed consent; 2. Patients with extremely high body weight (> 200 kg); 3. Patients who cannot cooperate to complete the transfer; 4. Patients who were enrolled in other interventional clinical trials that may have interfered with the results of this study; 5. Patients who could not understand or cooperate with the study process; 6. Have other conditions that, in the judgment of the investigator, are not suitable for participation in the trial; Health care workers: 1. Suffering from physiological (such as menstrual period, pregnancy) low back pain; 2. Suffering from pathological low back pain, such as tumor, tuberculosis, rheumatoid arthritis, visceral organ referred pain, ankylosing spondylitis, scoliosis, etc. 3. Healthcare professionals who have been enrolled in other interventional clinical trials that may interfere with the results of this study; 4. Have other conditions that, in the investigator's judgment, are not suitable for participation in the trial;

Design outcomes

Primary

MeasureTime frame
Incidence of adverse events in transit;

Secondary

MeasureTime frame
Comfort and safety evaluation;Transfer efficiency;Improvement of occupational health of medical staff;

Countries

China

Contacts

Public ContactTianlong Wang

Xuanwu Hospital Capital Medical University

w_tl5595@hotmail.com+86 10 83199333

Outcome results

None listed

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