Investigating Almond effect on bed sore

Not Applicable

Recruiting

• Conditions: Bedsore.; Pressure ulcer of unspecified elbow; L89.00

• Registration Number: IRCT20171128037657N1
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

Gain score 18 or less according to Braden criterion
Having at least 18 years of age and a maximum of 85 years

Exclusion Criteria

Dermatological allergy to drugs
Having a bed sore
Dissatisfaction with the patient or legal guardian
Having a skin disease
Receive any other topical ointment in the pressure areas
Skin sensitivity to almond and its products

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Percentage of people with bed sore. Timepoint: Daily review of the site for compression injuries for 7 days. Method of measurement: The National Pressure Ulcer Advisory Panel (NPUAP) is used.