- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04845672
Comparison of the Permanent Skin Flora of Children Who Had Bathing With Two Different Products
April 14, 2021 updated by: cagri covener ozcelik, Marmara University
Comparison of the Permanent Skin Flora of Children Who Had Bathing With Two Different Products: A Randomized Controlled Study
This study was carried out as a randomized controlled experimental study to compare the effect of wiping bath with 2% daily chlorhexidine gluconate and soap-free body wash on the permanent skin flora of children hospitalized in the PICU.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Microbiota to the ecosystem formed by symbiotic and pathogenic microorganisms (bacteria, fungi, viruses, archaea, etc.) living in and on the surface of the human body; All of the genes encoding them have been called the microbiome (Whitman et al., 1998).
The relationship between microbiota and many diseases that will have important consequences in human life has been proven.
Infection and infectious diseases increase the risk of developing complications in critically ill patients, sometimes followed by death.
Microbiota in healthy individuals contains many different microorganisms.
The microbiota that begins to form immediately after birth varies according to nutrition, genetics, age and geographic region and climate.
Human microbiota may change after applications such as infections, use of antibiotics, various chemicals (antiseptic solutions, soaps, shampoos, etc.).
This study was planned to compare the effect of wiping bath with 2% daily chlorhexidine gluconate and soap-free body washing solution on the skin microbiota of the patients hospitalized in the PICU.
This research will be done as a randomized controlled experimental.
The research population consists of 30 pediatric patients hospitalized in the Pediatric Intensive Care Unit of the Health Sciences University Umraniye Training and Research Hospital in 2021, who were wiped with 2% chlorhexidine gluconate, and 30 who were wiped with a soap-free body wash solution.
Power analysis was erformed using the G * Power (v3.1.7)
program to determine the number of samples.
The strength of the study is expressed as 1-β (= type II error probability) and generally the studies should have 80% power.
According to Cohen's effect size coefficients; Assuming that the evaluations to be made between two independent groups will have a large effect size (d = 0.8), it was decided to recruit 30 people, considering that there should be at least 26 people in each group at the level of α = 0.05 and there might be losses in the working process.
The research sample was randomly divided into branches; group I will consist of 30 patients and group II will consist of 30 patients.
Children in Group I will be applied soap-free body washing solution and children in Group II will be applied a wipe bath with 2% chlorhexidinegluconate, which is the routine application of the unit.
In both groups, swab samples will be taken from the right armpit and right groin before and after the wipe bath (6th hour).
'' Child Identification Form'' and ''Wipe Bathroom Application Chart'' will be used to collect data.
The Child Diagnostic Form consists of questions containing information about the child (age, gender, reason for hospitalization, date, etc.).
It is planned to record information on the wiping bath application schedule, the skin reactions that may occur in the patient during the wiping bath and the effect on the skin flora in the swab samples taken before and after the children's bath applications.
Data collection tools will be filled in by the researcher through observation.
During the data collection process, it was decided by the researcher to take swab samples before each wipe bath application and after the wipe bath application (6th hour) in order to check whether there was growth in the skin flora of the child's armpit and groin areas.
Before the research, the parents of the participants will be informed about the research and verbal / written consent will be obtained from the parents declaring their acceptance to participate in the study.
Collected data will be evaluated using the SPSS Statistics 22 package program.
At the end of the study, it is thought that it will guide the improvement of patient care quality.
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Çağrı Özçelik, PhD
- Phone Number: +905327484745
- Email: ccovener@gmail.com
Study Contact Backup
- Name: Berna Turan, BSC
- Phone Number: 00905382609668
- Email: bernaturan1@gmail.com
Study Locations
-
-
Maltepe
-
Istanbul, Maltepe, Turkey, 34854
- Recruiting
- Çağrı Çövener Özçelik
-
Contact:
- Çağrı Çövener Özçelik
- Phone Number: 05327484745
- Email: ccovener@gmail.com
-
Principal Investigator:
- Berna Turan, BSC
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 month to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being in the first 24 hours of admission to the PICU
- Internal reasons for hospitalization with children
- No co-morbid disease
- Hospitalization in PICU during data collection procedure
Exclusion Criteria:
- Hospitalization just before the study
- The children who is not available for wiping bath
- Hospitalized children after surgical procedures
- Antibotic use during the study
- Being chlorhexidine gluconate allergy history
- Impaired skin integrity (burns, skin disease etc.)
- Use of antibiotics, probiotics or steroid-containing immune system suppressing agents at last two months
- Radiotherapy or the chemotherapy patients
- Severe septic shock
- The children with tracheostomy, PEG, permanent dialysis catheter etc.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: 2% chlorhexidine gluconate
4% Chlorhexidine gluconate solution and one to one water will be used to create a 2% Chlorhexidine gluconate solution.
|
Children in 2% chlorhexidine gluconate group , which is the routine practice of the hospital, and a wiping bath in accordance with the bath protocol specified.
The bath procedure will take 10-15 minutes.
Before wiping bath swab sample will provide from armpit and groin with circular manner and 6 hours later swap sample will be provided from the same areas again.
The swab sample taken will be planted on blood agar medium and kept at + 4-8 ℃ for an average of 18-24 hours.
After it is planted on blood agar medium, it will be kept at + 4-8 ℃ for an average of 18-24 hours .
A total of 12 swab samples will be taken for 3 days from each child and from the same areas, body flora will be evaluated.
|
|
ACTIVE_COMPARATOR: soap-free body cleaning solution
It supports and protects the natural barrier function of the skin's natural protective layer.
|
Children in a wiping bath with soap-free body washing solution group, and a wiping bath in accordance with the bath protocol specified.
The bath procedure will take 10-15 minutes.
Before wiping bath swab sample will provide from armpit and groin with circular manner and 6 hours later swap sample will be provided from the same areas again.
The swab sample taken will be planted on blood agar medium and kept at + 4-8 ℃ for an average of 18-24 hours.
After it is planted on blood agar medium, it will be kept at + 4-8 ℃ for an average of 18-24 hours .
A total of 12 swab samples will be taken for 3 days from each child and from the same areas, body flora will be evaluated.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
permanent skin flora
Time Frame: 3 days
|
Blood Agar Base will be used to evaluate permanent skin flora
|
3 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Costello EK, Lauber CL, Hamady M, Fierer N, Gordon JI, Knight R. Bacterial community variation in human body habitats across space and time. Science. 2009 Dec 18;326(5960):1694-7. doi: 10.1126/science.1177486. Epub 2009 Nov 5.
- Chow J, Lee SM, Shen Y, Khosravi A, Mazmanian SK. Host-bacterial symbiosis in health and disease. Adv Immunol. 2010;107:243-74. doi: 10.1016/B978-0-12-381300-8.00008-3.
- Clemente JC, Ursell LK, Parfrey LW, Knight R. The impact of the gut microbiota on human health: an integrative view. Cell. 2012 Mar 16;148(6):1258-70. doi: 10.1016/j.cell.2012.01.035.
- Elias PM. Stratum corneum defensive functions: an integrated view. J Invest Dermatol. 2005 Aug;125(2):183-200. doi: 10.1111/j.0022-202X.2005.23668.x.
- Human Microbiome Project Consortium. A framework for human microbiome research. Nature. 2012 Jun 13;486(7402):215-21. doi: 10.1038/nature11209.
- Karki S, Cheng AC. Impact of non-rinse skin cleansing with chlorhexidine gluconate on prevention of healthcare-associated infections and colonization with multi-resistant organisms: a systematic review. J Hosp Infect. 2012 Oct;82(2):71-84. doi: 10.1016/j.jhin.2012.07.005. Epub 2012 Aug 11.
- Grice EA, Segre JA. The skin microbiome. Nat Rev Microbiol. 2011 Apr;9(4):244-53. doi: 10.1038/nrmicro2537. Erratum In: Nat Rev Microbiol. 2011 Aug;9(8):626.
- Kong HH, Segre JA. Skin microbiome: looking back to move forward. J Invest Dermatol. 2012 Mar;132(3 Pt 2):933-9. doi: 10.1038/jid.2011.417. Epub 2011 Dec 22.
- Whitman WB, Coleman DC, Wiebe WJ. Prokaryotes: the unseen majority. Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6578-83. doi: 10.1073/pnas.95.12.6578.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
February 15, 2021
Primary Completion (ANTICIPATED)
February 15, 2022
Study Completion (ANTICIPATED)
February 15, 2022
Study Registration Dates
First Submitted
April 11, 2021
First Submitted That Met QC Criteria
April 11, 2021
First Posted (ACTUAL)
April 15, 2021
Study Record Updates
Last Update Posted (ACTUAL)
April 19, 2021
Last Update Submitted That Met QC Criteria
April 14, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01/28
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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