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

Comparison between the effect of Aleo Vera and Olive Oil preventive dressing usage on pressure injury development in critically ill patients who admitted to intensive care unit (ICU) of Velayat Teaching Hospital, Qazvin.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200105046008N1
Enrollment
90
Registered
2020-08-05
Start date
2020-02-20
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

Pressure injury. Pressure ulcer

Interventions

Intervention 1: Intervention group: The patients' skin is examined twice a day for 7 days and the sacrum area will be bandaged using an aloe vera gel preventive dressing. Regarding the dressing and th
Thus, the preventive dressing consists of a simple gas measuring 5 cm2 impregnated with 5 cc of aloe vera, which will be used in the anatomical region of the sacrum to prevent pressure injury. It shou
Thus, the preventive dressing consists of a simple gas measuring 5 cm2 impregnated with 5 cc of olive oil, which will be used in the anatomical region of the sacrum to prevent pressure injury. It shou

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Pressure injury. Timepoint: Twice, everyday for 7 day. Method of measurement: Pressure injury staging system.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnoosh Rashvand

Qazvin University of Medical Sciences

n.rashvand@yahoo.com+98 912 118 3026

Outcome results

None listed

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