pressure ulcer.
Conditions
Interventions
Intervention group: Intervention group: The first intervention group consisted of hydrocolloid dressing and the second intervention group, including transparent film dressing and control group.
Sponsors
Gonabad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Having informed consent to attend research The need for oxygen therapy for more than two hours through nasal cannula and facial mask Age older than 18 years The absence of ulcers in the patient's ears and having healthy ears
Exclusion criteria
Exclusion criteria: Cancellation of the patient, but the patient's cure at any time of the study Discontinue oxygen therapy during the study according to the physician's order Discharge or transfer of patient
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pressure ulcer. Timepoint: The effect of hydrocolloid dressing and film cloth will be checked for three days and twice a day. Method of measurement: Braden Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Braden Scale. Timepoint: Before the intervention begins. Method of measurement: Braden Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNeda Sabahi
Gonabad University of Medical Sciences
Outcome results
None listed