- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07421323
Chlorhexidine Gluconate and Alcohol Hand Rubbing on Healthcare-associated Infection
February 12, 2026 updated by: Marwa Mohamed Farag, Alexandria University
a Comparison Between Effect of Chlorhexidine Gluconate and Alcohol Hand Rubbing on Healthcare-associated Infection
This study aims to compare of effect of chlorhexidine gluconate and alcohol hand rubbing on healthcare-associated infection (HCAI) in neonatal intensive care unit at Alexandria University Children Hospital.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
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 Locations
-
-
-
Alexandria, Egypt, 0325
- Recruiting
- Marwa Mohamed Farag
-
Contact:
- Marwa M Farag
- Phone Number: 01143193333
- Email: d.marwa.farag@gmail.com
-
Contact:
- Hoda Ewiss, MD
- Email: h_soliman20110@alexmed.edu.eg
-
-
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
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
Neonates <37 weeks gestational age admitted to NICU of Alexandria University Children's Hospitals
Exclusion Criteria:
Patients with any of the following will be excluded:
- Obvious major congenital abnormalities, immunodeficiency and inborn error of metabolism.
- Early onset sepsis (before the third day).
- Infants more than 72 hours of age at the time of randomization.
- Parental consent lacking/refusal.
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 Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Alcohol hand rub
Medical staff used chlorhexidine in hand rubs before contacting the neonates during their hospital stay.
|
Medical staff used alcohol in hand rubs before contacting the neonates during their hospital stay.
|
|
Active Comparator: chlorohexidine hand rub
Medical staff used alcohol in hand rubs before contacting the neonates during their hospital stay.
|
Medical staff used Chlorhexidine in hand rubs before contacting the neonates during their hospital stay.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
blood culture
Time Frame: first month of life
|
having blood culture from studied groups on day 7, 14, and 28 after birth.
|
first month of life
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
August 1, 2025
Primary Completion (Estimated)
March 1, 2026
Study Completion (Estimated)
April 1, 2026
Study Registration Dates
First Submitted
February 12, 2026
First Submitted That Met QC Criteria
February 12, 2026
First Posted (Actual)
February 19, 2026
Study Record Updates
Last Update Posted (Actual)
February 19, 2026
Last Update Submitted That Met QC Criteria
February 12, 2026
Last Verified
August 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 010820
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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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