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Effect evaluation of evidence application in prevention of medical device related pressure injury in critical patients

Knowledge to Action Framework in prevention of medical device related pressure injury in critical patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040117
Enrollment
Unknown
Registered
2020-11-21
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-01-11

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

Conditions

medical device related pressure injury

Interventions

control group:Routine care
Experimental group:prevention approach

Sponsors

TianJin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. There was no medical device-related pressure injury at admission; 2. Risk of MDRPI, i.e. continuous use of any one or more medical devices such as ECG monitoring cuff and or electrode plate, oxygen mask, nasal catheter, tracheal tube, urinary tube, nasogastric tube, restraint belt and other medical devices, and the duration is > 12h; 3. Aged >= 18 years old; 4. Braden score <=12; 5. Informed consent of patients or family members.

Exclusion criteria

Exclusion criteria: 1. Patients who are not allowed to change their position due to their condition; 2. Those who are confused and unable to cooperate; 3. Those who were unable to complete the study due to discharge or death.

Design outcomes

Primary

MeasureTime frame
incidence of MDRPI;—

Countries

China

Contacts

Public ContactWeiLi
weili066100@126.com+86 02260118816

Outcome results

None listed

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