Trial Review

The ANZCTR website is back online for trial registration and updates. We apologise for any inconvenience caused while the site was inactive.


With activity expected to increase on the ANZCTR again, there may be extended wait times while we process pending studies, with priority being given to those trials submitted in February. Thank you for your patience.


Reset your password and enable multi-factor authentication (MFA)


For ANZCTR account holders: to help ensure the cyber safety of your account, you’ll need to reset your password and set-up multi-factor authentication (MFA) as per the instructions below.


  1. Go to the Login page, click ‘reset password’ and follow the instructions.
  2. Check your email for the link to set a new password.
  3. Create a new password that meets requirements.
  4. Return to the Login page and enter your new password. A verification code will be sent to your email.
  5. Check your email for the code and enter it on the Login page. If the code is entered incorrectly, you can re-enter the correct one or request a new one.

Learn more about MFA and its importance on the Australian Signals Directorate website.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12623000752662
Ethics application status
Approved
Date submitted
30/03/2023
Date registered
11/07/2023
Date last updated
16/12/2024
Date data sharing statement initially provided
11/07/2023
Type of registration
Prospectively registered

Titles & IDs
Public title
Comparison of early versus late initiation of trophic feeding in preterm infants.
Scientific title
Comparison of early versus late initiation of trophic feeding in preterm infants on duration of stay in high dependency unit: a non-randomized clinical trial
Secondary ID [1] 308774 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
prematurity 328736 0
Condition category
Condition code
Oral and Gastrointestinal 325736 325736 0 0
Normal oral and gastrointestinal development and function
Reproductive Health and Childbirth 327407 327407 0 0
Other reproductive health and childbirth disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Early trophic feed initiation will be done according to birth date admitted on their 1st or 2nd day of life comprising of expressed breast milk given at <48 hours postntal age of preterm infant every 2 hourly 1 to 2 ml in amount with a total of 12 feeds in 24 hours. Increasing the amount of feed daily by 1-2 ml till the end of stay or when neonate is able to take full oral feeds.
Intervention code [1] 325237 0
Prevention
Comparator / control treatment
Late trophic feed initiation will be done according to birth date admitted on their 3rd day of life comprising of expressed breast milk given at > 72 hours postnatal age of preterm infant 1 to 2 ml in amount administered 2 hourly with a total of 12 feeds in 24 hours.
Increasing the amount of feed daily by 1 to 2ml till the end of stay or till the preterm infant is able to tolerate full oral feeds.
Control group
Active

Outcomes
Primary outcome [1] 333586 0
Duration of stay of preterm infant in neonatal high dependency unit determined from hospital records.
Timepoint [1] 333586 0
Duration of stay of preterm infant in neonatal high dependency unit assessed in days at the time of hospital discharge.
Secondary outcome [1] 417647 0
Improved preterm survival in neonatal high dependency unit determined from hospital records.
Timepoint [1] 417647 0
At the time of discharge from neonatal high dependency unit of hospital.

Eligibility
Key inclusion criteria
Preterm 28 weeks to 36 weeks gestation.
Birth weight 1000 to 2500 g
Age<3 days postnatal age at time of admission
Minimum age
1 Days
Maximum age
2 Days
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Preterm infants with major congenital anomaly.
Preterm infant on inotropic drug support.
Preterm infants with severe respiratory distress.

Study design
Purpose of the study
Prevention
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Allocation by birth date
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
t test is used to compare the duration of stay in high dependency unit of both groups.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
30/07/2023
Actual
30/07/2023
Date of last participant enrolment
Anticipated
30/10/2023
Actual
30/10/2023
Date of last data collection
Anticipated
20/11/2023
Actual
25/11/2023
Sample size
Target
240
Accrual to date
Final
240
Recruitment outside Australia
Country [1] 25217 0
Pakistan
State/province [1] 25217 0
Khyber Pakhtunkhwa

Funding & Sponsors
Funding source category [1] 312995 0
Hospital
Name [1] 312995 0
Lady reading hospital
Country [1] 312995 0
Pakistan
Primary sponsor type
Hospital
Name
Lady Reading Hospital
Address
Paediatric ward MTI LRH Peshawar, Soekarno Rd, PTCL Colony Peshawar, Khyber Pakhtunkhwa 25000, Pakistan.
Country
Pakistan
Secondary sponsor category [1] 314677 0
None
Name [1] 314677 0
Address [1] 314677 0
Country [1] 314677 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 312259 0
Institutional Review Board,MTI LRH Peshawar
Ethics committee address [1] 312259 0
Ethics committee country [1] 312259 0
Pakistan
Date submitted for ethics approval [1] 312259 0
22/02/2023
Approval date [1] 312259 0
08/03/2023
Ethics approval number [1] 312259 0
678/LRH/MTI

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 124018 0
A/Prof Rabiya Munir
Address 124018 0
Paediatric ward LRH, Paediatric ward MTI LRH Peshawar, Soekarno Rd, PTCL Colony Peshawar, Khyber Pakhtunkhwa 25000, Pakistan.
Country 124018 0
Pakistan
Phone 124018 0
+923465324232
Fax 124018 0
Email 124018 0
[email protected]
Contact person for public queries
Name 124019 0
Rabiya Munir
Address 124019 0
Paediatric ward LRH, Paediatric ward MTI LRH Peshawar, Soekarno Rd, PTCL Colony Peshawar, Khyber Pakhtunkhwa 25000, Pakistan.
Country 124019 0
Pakistan
Phone 124019 0
+923465324232
Fax 124019 0
Email 124019 0
[email protected]
Contact person for scientific queries
Name 124020 0
Rabiya Munir
Address 124020 0
Paediatric ward LRH, Paediatric ward MTI LRH Peshawar, Soekarno Rd, PTCL Colony Peshawar, Khyber Pakhtunkhwa 25000, Pakistan.
Country 124020 0
Pakistan
Phone 124020 0
+923465324232
Fax 124020 0
Email 124020 0
[email protected]

Data sharing statement
Will the study consider sharing individual participant data?
No


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
18663Ethical approval  [email protected] Ethical approval.jpg
18664Statistical analysis plan  [email protected] Statistical analysis plan.docx
18665Study protocol  [email protected] Study Protocol.docx
18666Informed consent form  [email protected] Consent form-Preterm.docx
18765Other  [email protected] Data collectionproforma DATA COLLECTION PROFORMA-PRETERM.docx



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.