bed sores. Pressure ulcer
Conditions
Interventions
Intervention 1: Control group: Study samples will be treated with a dressing impregnated with 2% progesterone and zinc oxide combined cream twice per day until the wound heals. Intervention 2: Interve
Sponsors
Yazd University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: patients with pressure ulcers Age over 18 years Satisfaction to participate in the study
Exclusion criteria
Exclusion criteria: Patients with a variety of female pathological diseases pregnancy Patients in critical condition that the relevant specialist does not allow them to participate in the study Known allergy to progesterone
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of involvement with bed sores. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: clinical examination.;Wound grade in patients. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: clinical examination.;Mean wound size and depth in patients. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: clinical examination.;Existence of infection and discharge from wounds in patients with bed sores. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: clinical examination.;Pain or sensation at the site of the ulcer. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: clinical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactReza Zare Modouiei
Yazd University of Medical Sciences
Outcome results
None listed