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Clinical Trials/NCT06330506
NCT06330506
Recruiting
Not Applicable

The Effect of Pressure Ulcer Care Package on the Risk of Surgery-Related Pressure Ulcer Development in Patients Undergoing Orthopaedic Surgery

Cukurova University1 site in 1 country102 target enrollmentApril 10, 2024
ConditionsPressure Ulcer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pressure Ulcer
Sponsor
Cukurova University
Enrollment
102
Locations
1
Primary Endpoint
Evaluation of pressure ulcer formation
Status
Recruiting
Last Updated
last year

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
April 10, 2024
End Date
September 10, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sevgi Deniz Dogan

assistant professor

Cukurova University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Evaluation of pressure ulcer formation

Time Frame: Three days later

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.In this Form, pressure wound stages are classified into stages: Stage I, II, III, IV, Unstageable, Deep Tissue, and Mucosal Membrane Pressure Wound.

Study Sites (1)

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