Topical Emollient Therapy
Primary Purpose
Blood Stream Infection
Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Topical Emollient
Sponsored by
About this trial
This is an interventional prevention trial for Blood Stream Infection focused on measuring Topical Emollient Therapy, Emollient, Preterm, Hospital Acquired Infection
Eligibility Criteria
Inclusion Criteria:
- Any preterm neonates (>26 weeks and < 37 weeks of gestation by maternal dates)
- Birth weight of at least 750 gm
- Age ≤72 hours of life
- Baseline blood cultures obtained
- Expected survival > 48 hours (based on the clinical judgment by the physicians)
Exclusion Criteria:
- Neonate with severe RDS on admission as declared by the consulting Physician on the basis of radiologic findings.
- Neonate within first 24 hours of critical care
- Life threatening congenital anomalies
- Congenital skin anomalies
- Hydrops Fetalis
- Congenital infection of the skin
- History of any previous treatment with the ointment
- Newborns admitted for major surgical procedure with expected high rates of infectious complications.
- Newborns with positive baseline blood cultures
Sites / Locations
- The Aga Khan University
- The Aga Khan University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Topical Emollient
Routine Skin Care
Arm Description
Neonates in this group will receive topical emollient application with coconut oil twice a day till 28th day of life
Neonates in this group will receive routine skin care as per unit protocol
Outcomes
Primary Outcome Measures
Hospital Acquired Blood Stream Infection
Hospital Acquired Infection is defined as a blood culture positive for any organism in a neonate with baseline negative cultures on admission.
Secondary Outcome Measures
Weight Gain
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01396642
Brief Title
Topical Emollient Therapy
Official Title
Effect of Topical Emollient Therapy on Clinical Outcomes in Preterm Neonates - A Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aga Khan University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Almost all (99%) of the neonatal deaths occur in lower and middle income countries. Most of these deaths are attributable to prematurity and infection. With the increasing rate of premature births in some settings, the mortality rate of over 50% among preterm babies in some of the developing countries require inexpensive hospital-based strategies to prevent fatal infections in newborns of these countries. As most of the deaths in preterm neonates are attributable to their vulnerability of infection, a potential low cost intervention like topical emollient therapy can be effectively directed to reduce infection related mortality and morbidity in the developing countries. Topical emollient therapy reduces the rate of infection by enhancing the skin barrier function, thus reducing trans-epidermal water loss consequently conserving heat and energy to promote growth.
The broad goal of the study is to improve the survival rate of hospitalized preterm neonates in the developing countries by decreasing the incidence of infection using low-cost interventions.
HYPOTHESIS:
It is hypothesized that topical emollient therapy with coconut oil twice a day till 28th day of life in hospitalized preterm neonates reduces the incidence proportion of hospital acquired infection by 40% 15 as compared to routine skin care. For the secondary objective it is hypothesized that the weight gain in the neonates receiving prophylactic application of emollient, which is coconut oil twice a day till 28th day of life, is at least 2g/kg/day18 more as compared to the weight gain in the routine skin care group.
Detailed Description
Research question:
The primary research question to be addressed via this study is whether the prophylactic application of emollient, which is coconut oil twice a day till 28th day of life, effective in reducing the incidence proportion of hospital acquired infection among preterm neonates by 40% as compared to the routine skin care.
The secondary research question is whether the weight gain in the neonates receiving prophylactic application of emollient, which is coconut oil twice a day till 28th day of life, is at least 2g/kg/day more as compared to the weight gain in the routine skin care group.
Objectives: This study has the following primary objectives:
To evaluate the effectiveness of topical emollient in preventing hospital acquired infection in preterm neonates.
The secondary objective is:
To compare the weight gain among the two groups of neonates.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blood Stream Infection
Keywords
Topical Emollient Therapy, Emollient, Preterm, Hospital Acquired Infection
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
258 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Topical Emollient
Arm Type
Experimental
Arm Description
Neonates in this group will receive topical emollient application with coconut oil twice a day till 28th day of life
Arm Title
Routine Skin Care
Arm Type
No Intervention
Arm Description
Neonates in this group will receive routine skin care as per unit protocol
Intervention Type
Other
Intervention Name(s)
Topical Emollient
Intervention Description
Neonates in this group will receive topical emollient application with coconut oil twice a day till 28th day of life
Primary Outcome Measure Information:
Title
Hospital Acquired Blood Stream Infection
Description
Hospital Acquired Infection is defined as a blood culture positive for any organism in a neonate with baseline negative cultures on admission.
Time Frame
28 days of life
Secondary Outcome Measure Information:
Title
Weight Gain
Time Frame
28th Day of Life
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Minutes
Maximum Age & Unit of Time
72 Hours
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Any preterm neonates (>26 weeks and < 37 weeks of gestation by maternal dates)
Birth weight of at least 750 gm
Age ≤72 hours of life
Baseline blood cultures obtained
Expected survival > 48 hours (based on the clinical judgment by the physicians)
Exclusion Criteria:
Neonate with severe RDS on admission as declared by the consulting Physician on the basis of radiologic findings.
Neonate within first 24 hours of critical care
Life threatening congenital anomalies
Congenital skin anomalies
Hydrops Fetalis
Congenital infection of the skin
History of any previous treatment with the ointment
Newborns admitted for major surgical procedure with expected high rates of infectious complications.
Newborns with positive baseline blood cultures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zulfiqar ZB Bhutta, MBBS, PhD
Organizational Affiliation
The Aga Khan University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rehana A Salam, MSc
Organizational Affiliation
The Aga Khan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Aga Khan University
City
Karachi
State/Province
Sindh
ZIP/Postal Code
74800
Country
Pakistan
Facility Name
The Aga Khan University
City
Karachi
State/Province
Sindh
Country
Pakistan
12. IPD Sharing Statement
Citations:
PubMed Identifier
25637007
Citation
Salam RA, Darmstadt GL, Bhutta ZA. Effect of emollient therapy on clinical outcomes in preterm neonates in Pakistan: a randomised controlled trial. Arch Dis Child Fetal Neonatal Ed. 2015 May;100(3):F210-5. doi: 10.1136/archdischild-2014-307157. Epub 2015 Jan 30.
Results Reference
derived
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Topical Emollient Therapy
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