Evaluation of 2% progesterone cream efficacy in the treatment of patients with bed sores

Phase 2

• Conditions: bed sores.; Pressure ulcer

• Registration Number: IRCT20190810044500N24
• Lead Sponsor: Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 8 March 2022

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 44

Inclusion Criteria

patients with pressure ulcers
Age over 18 years
Satisfaction to participate in the study

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.