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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06330506
Other study ID # 123456123456
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 10, 2024
Est. completion date September 10, 2024

Study information

Verified date March 2024
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to determine the effect of pressure ulcer care package use on the risk of pressure ulcer development due to surgery in patients undergoing orthopedic surgery. It was planned as a randomized controlled study. The population of the study will consist of patients who underwent surgery in the Orthopaedics and Traumatology Clinic of Doğubayazıt Dr.Yaşar Eryılmaz State Hospital Hospital Hospital of Ağrı Provincial Health Directorate. The sample of the study will consist of patients who volunteered to participate in the study that meets the inclusion criteria. To obtain research data, the Personal Information Form developed by the researcher in line with the literature, 3S Operating Theatre Pressure Wound Risk Assessment Scale, Pressure Wound Regions and Stages Monitoring Form prepared according to NPUAP (2016) Pressure Wound Staging System Form will be used. Statistical analysis of the data obtained from the study will be performed using the SPSS 25 (Statistical Package of Social Science) package program.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 102
Est. completion date September 10, 2024
Est. primary completion date August 10, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Orthopaedics and traumatology department - Those who have undergone general or spinal anesthesia - Without any communication problems - Patients who volunteered to participate in the study Exclusion Criteria: - Patients with pre-operative pressure ulcer - Those who are bedridden - Patients referred to the intensive care unit after surgery - Patients who wish to leave the study will be excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pressure ulcer prevention pack
The pressure ulcer prevention package to be prepared by the researchers will be applied

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of pressure ulcer formation The 'Pressure Ulcer Sites and Stages Follow-up Form' created by the researchers will be used. With this form, pressure ulcer stages and regions of the patients will be monitored. Three days later
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