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Trial registered on ANZCTR
Registration number
ACTRN12619001601123p
Ethics application status
Submitted, not yet approved
Date submitted
22/07/2019
Date registered
20/11/2019
Date last updated
20/11/2019
Date data sharing statement initially provided
20/11/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Validity of CRIB II scoring system and mean platelet volume to predict mortality in preterm infants
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Scientific title
Validity of CRIB II scoring system and mean platelet volume to predict mortality in preterm infants
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Secondary ID [1]
298799
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NIL
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Universal Trial Number (UTN)
U1111-1237-3486
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Preterm infants
314262
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Neonatal mortality
314263
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Condition category
Condition code
Emergency medicine
312163
312163
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0
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Other emergency care
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Reproductive Health and Childbirth
312164
312164
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0
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Other reproductive health and childbirth disorders
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Studying the variables that potentially influence the neonatal mortality rates amongst preterm infants within the neonatal intensive care unit NICU environment would enrich the health care quality control and rational use of resources. Clinical Risk Index for Babies scoring system (CRIB II) is a recently developed tool to predict the risk of mortality in preterm infants admitted to NICU. Mean platelet volume (MPV) of preterm infants admitted to NICU was examined in previous studies correlating with occurrence of early onset sepsis and predicting neonatal mortality. The aim of the current study is to examine the validity of CRIB II scoring system and MPV separately and combined to predict preterm infant mortality at NICU, Dubai Hospital. It is a retrospective study and data will be retrieved from medical records of all preterm infants less than 32 weeks of gestation who were admitted to NICU over a period of two years from July 2017 to July 2019. A data collection tool covering the basic elements of CRIB II score will be created and includes; sex, gestational age, weight, admission temperature and base excess extracted from the blood gas result on admission. Mean platelet volume data will be also retrieved from the first complete blood count result collected shortly after admission. CRIB II score will be calculated for all enrolled infants in the first 24 hours of life and the validity of CRIB II score separately and in combination with MPV to predict the neonatal mortality risk amongst preterm infants will be evaluated.
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Intervention code [1]
315077
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Diagnosis / Prognosis
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Comparator / control treatment
no control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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risk of mortality among preterm infants admitted to NICU. Mortality rate will be retrieved from
medical records data of admitted infants to NICU.
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Assessment method [1]
320805
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Timepoint [1]
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First 24 hours of admission
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Secondary outcome [1]
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Prediction validity of CRIB II score for Length of hospital stay among preterm infants. CRIB II scoring will be calculated from a data collection tool and includes gestational age, birth weight, gender, base excess determined from blood gas analysis, and admission temperature. Scores will be calculated and compared to the observed mortality. Validity will be assessed by calculating the receiver operating characteristic curve and the associated area under the curve.
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Assessment method [1]
372909
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Timepoint [1]
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Death up to 28 days after birth
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Eligibility
Key inclusion criteria
All preterm infants between 24- 32 weeks of gestation admitted to NICU during the study period
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Minimum age
2
Hours
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Maximum age
24
Hours
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
-preterm infants weighing less than 500 Gm
-Major congenital anomalies
-Genetic disorders
-Major surgical problems
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Study design
Purpose
Screening
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Retrospective
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Statistical methods / analysis
Sample size will be determined by the rate of admission to NICU during the study period as all eligible preterm infants will be enrolled.
-The quantitative variables will be evaluated according to mean and standard deviation, median, and maximum and minimum scores. The t Student test Will be applied when gestational age is evaluated to compare the infants who survived with those that died. Associations of the categorized variables with neonatal death will be evaluated utilizing the Chi square test. The cut-off points for neonatal mortality through the CRIB II score, BW, GA, and MPV will be evaluated by the Receiver Operator Characteristic curve
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
5/01/2020
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Actual
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Date of last participant enrolment
Anticipated
16/05/2020
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Actual
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Date of last data collection
Anticipated
28/06/2020
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Actual
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Sample size
Target
200
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
21708
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United Arab Emirates
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State/province [1]
21708
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Dubai
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Funding & Sponsors
Funding source category [1]
303357
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Hospital
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Name [1]
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dubai hospital
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Address [1]
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Nicu, Dubai Hospital.
Third floor. Al-baraha,
Alkornisch street No.1.
Dubai 7272 .
United Arab Emirates.
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Country [1]
303357
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United Arab Emirates
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Primary sponsor type
Hospital
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Name
Dubai Hospital
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Address
Nicu, Dubai Hospital.
Third floor. Al-baraha,
Alkornisch street No.1.
Dubai 7272 .
United Arab Emirates.
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Country
United Arab Emirates
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
303387
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Country [1]
303387
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Ethics approval
Ethics application status
Submitted, not yet approved
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Ethics committee name [1]
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Dubai scientific research ethics committee DSREC
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Ethics committee address [1]
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Dubai Scientific Research Ethics Committee DSREC. DSREC Continuous Medical Education Department Rashid Medical Library, PO BOX 4545 Dubai. UAE
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Ethics committee country [1]
303887
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United Arab Emirates
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Date submitted for ethics approval [1]
303887
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11/07/2019
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Approval date [1]
303887
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Ethics approval number [1]
303887
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Summary
Brief summary
Advances in perinatal medicine and improved supportive and therapeutic modalities within neonatal intensive care units (NICU) have led to significant decline in neonatal mortality rates among preterm infants. Studying the different variables that may influence mortality rates in NICU could give valuable information and enrich the data base that improves quality control standards. Clinical Risk Index for Babies scoring system (CRIB II) is a recently developed tool to predict risk of mortality amongst preterm infants admitted to NICU. Mean platelet volume MPV) was studied previously as a promising sensitive marker of early onset neonatal sepsis and neonatal mortality.The aim of the current study is to examine the validity of CRIB II scoring system compared to mean platelet volume (MPV) to predict the risk of preterm infant mortality at NICU. It is a retrospective observational study during the period between June 2017 until June 2019. All preterm neonates with gestational age 24 to 32 weeks and low birth weight <1500 gram admitted during the first 24 hours to the NICU; Dubai hospital will be included.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Atef Alshafei
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Address
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NICU, Dubai Hospital,
Third floor.
Al-baraha,
Alkornisch street No.1.
DUBAI 7272.
UAE
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Country
95130
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United Arab Emirates
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Phone
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+971561924270
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
95131
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Atef Alshafei
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Address
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NICU, Dubai Hospital,
Third floor.
Al-baraha,
Alkornisch street No.1.
DUBAI 7272.
UAE
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Country
95131
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United Arab Emirates
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Phone
95131
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+971561924270
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Fax
95131
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Email
95131
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[email protected]
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Contact person for scientific queries
Name
95132
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Atef Alshafei
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Address
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NICU, Dubai Hospital,
Third floor.
Al-baraha,
Alkornisch street No.1.
DUBAI 7272.
UAE
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Country
95132
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United Arab Emirates
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Phone
95132
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+971561924270
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Fax
95132
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Email
95132
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
All of the individual participant data collected during the trial.
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When will data be available (start and end dates)?
One month following main results publication. No end dates.
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Available to whom?
case by case basis
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Available for what types of analyses?
Any purpose
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How or where can data be obtained?
access subject to approvals by Principal Investigator, Contact email address:
[email protected]
-Contact mobile: 00971561924270
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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