The effect of silicone protective pad on pressure ulcer

Not Applicable

• Conditions: Patients undergoing cardiac surgery.; 120-125; 100-199

• Registration Number: IRCT2015110619919N3
• Lead Sponsor: Vice chancellor for research,Tabriz 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: Complete
• Sex: All
• Target Recruitment: 164

Inclusion Criteria

Willingness to participate in the study and signed an informed consent form; Age 75-30 years; Undergo bypass surgery for first time; No history of blood disorders; Having BMI 18.5 to 24.9; Connect to pump circulation outside the body; No history of bedsores.
Exclusion criteria: Long operation time more than 5 hours; emergency surgery; Having skin problems such as hives, swelling, redness and sensitivity to drugs and environmental factors in the area of Batks; Having Sensorimotor disability[Such as stroke].

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduce the incidence of pressure ulcers. Timepoint: Befor intervention, 24 and 48 hour after intervention and the time of discharge. Method of measurement: The measure Torrance Scale.

Secondary Outcome Measures

Name	Time	Method
-. Timepoint: -. Method of measurement: -.