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The effect of Aleo Vera and Olive Oil preventive dressing usage on pressure injury development.

Phase 3
Recruiting
Conditions
Pressure injury.
Pressure ulcer
Registration Number
IRCT20200105046008N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
90
Inclusion Criteria

The patient or his/her family's informed consent to participate in the study.
Aged above 18 years old.
The absence of pressure injury on arrival at ICU.
Patients with moderate to high risk based on the score they achieved from the Braden criterion at entry (score 14 and below).

Exclusion Criteria

Pressure injury development within the first 12 hours after entering the ward.
Conditions where the patient's position cannot be changed, such as patients with spinal cord injury.
Drug sensitivity to Aleo Vera in group 1 and Olive oil in group 2 (according to patient or if sensitivity was observed in the study).
Patient's death

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pressure injury. Timepoint: Twice, everyday for 7 day. Method of measurement: Pressure injury staging system.
Secondary Outcome Measures
NameTimeMethod
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