Behçet Uz Hospital
Izmir, Turkey (Türkiye)
NCT Number: NCT05686902
The aim of this study is to determine the effect of two different skin care solutions used in stoma care on peristomal skin integrity and compare them with each other.
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Notify Me1 day–18 year
All sexes
Interventional
Not applicable
Izmir, Turkey (Türkiye)
ABSTRACT
The research was planned as a randomized controlled experiment. Simple stratified randomization according to age will be done. The purpose of the study will be explained to the children and their parents who agreed to participate in the study and their consent will be obtained.
Study Groups: In the study, there will be 2 groups with 12 patients in each group.
Intervention Procedure: After obtaining written consent, peristomal skin integrity of all participants will be evaluated on day 0 post-op prior to randomization.
Peristomal Skin Integrity Assessment:
Statistical Analysis: A researcher who does not know which group the patients are in will perform the statistical analysis of the study using the single-blind method. Analysis of the data obtained from the research will be carried out in IBM® SPSS Statistics Version 22 program. Age, gender, etc. of the patients in the study. demographic characteristics will be given as number and percentage distributions. Comparisons of numerical variables between groups; It will be evaluated with a non-parametric or parametric appropriate test by looking whether the normal distribution condition is met. In the study, the statistical significance value was determined as p<0.05.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The difference in peristomal skin integrity between the groups will be examined.
Time frame: change between the 0th and the 7th day
skin pH measurement around stoma will be measured with a portable device brand BRD
Time frame: change between the 0th and the 7th day
Skin temperature measurement around stoma will be measured with a portable infrared device.
Time frame: change between the 0th and the 7th day
percent of (%)skin moisture around the soma will be measured with a portable device brand BRD
Time frame: change between the 0th and the 7th day
It is a 9-parameter evaluation scale developed by Joyce Pittman in 2014, and its validity and reliability in Turkish were performed by Arslantaş et al. in 2019. The purpose of the scale is to evaluate the frequency and severity of early postoperative complications during follow-up in individuals with stoma. This index Evaluates leakage, peristomal irritant dermatitis, pain, bleeding in or around the stoma, stomal necrosis, stenosis, retraction, mucocutaneous separation, and hyperplasia All complications 0 to 3 (0 = absent, 1 = mild, 2 = moderate, 3 = severe) (The total score ranges from 0 to 27. Higher scores indicate more severe ostomy complications)
Izmir Katip Celebi University
Other
Comparison of Two Different Solutions for Peristomal Skin Care in Patients With Pediatric Stoma: A Randomized Controlled Clinical Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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