Skip to content

The effect of silicone protective pad on pressure ulcer

The effect of silicone protective pad on pressure ulcers in patients undergoing coronary artery bypass

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015110619919N3
Enrollment
164
Registered
2016-04-11
Start date
2016-01-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients undergoing cardiac surgery. 120-125

Interventions

Intervention 1: Intervention group 1: In the intervention group, silicone protective pad with length of 90,width of 60 and a thickness of 3.5 cm for the prevention of pressure ulcers during surgery on
Prevention
Treatment - Other
Intervention group 1: In the intervention group, silicone protective pad with length of 90,width of 60 and a thickness of 3.5 cm for the prevention of pressure ulcers during surgery on the sacrum and
Cntrol group: The control group will not be any interference and these groups will receive the same care and routine Intervention.

Sponsors

Vice chancellor for research,Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAghal Moosa

School of Nursing and Midwifery- University of Medical Sciences

Aghalm6768@gmail.com+98 45323199

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026