Effectiveness of Nursing Recommendation of National Pressure Ulcer Advisory Panel on Prevention of Medical device–related pressure injury in Intensive Care Unit of Qazvin velayat Hospital

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200726048208N1

Enrollment

120

Registered

2020-08-05

Start date

2020-08-09

Completion date

Unknown

Last updated

2020-08-17

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

Conditions

Compression injury caused by medical device.

Interventions

Intervention 1: Intervention group: The second phase of astrology is performed one week after the first phase and in the same section in the intervention group. At this stage, 60 patients who meet the

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Informed consent of the patient or his family to participate in the research. Have at least one medical device attached to the patient

Exclusion criteria

Exclusion criteria: Restrictions on examining the skin under the device attached to the patient, for example, examining the skin under the neck in a patient with limited neck movement. Reluctance to participate in research If the equipment is removed within the first 24 hours, the patient is transferred to the ward or dies

Design outcomes

Primary

Measure	Time frame
Pressure injury. Timepoint: Interval 24 hours to 21 days. Method of measurement: Scale grading pressure ulcer.	—

Countries

Iran (Islamic Republic of)

Contacts

Public Contactlida shamekhi

Qazvin University of Medical Sciences

shamekhi1367@gmail.com+98 28 3322 3973

Outcome results

None listed

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