Arachidonic Acid Supplementation in Very Preterm Infants

July 17, 2015 updated by: Ayham alshweki, Health Research Institute of Santiago

Effects of Different Arachidonic Acid Supplementation on Psychomotor Development in Very Preterm Infants, a Randomized Controlled Trial

Long-chain polyunsaturated fatty acids (LCPUFAs), arachidonic acid (AA omega-6; 20:4ω-6), and docosahexaenoic acid (DHA omega-3; 22:6ω-3), are required for the formation of non-myelinated cell membranes in the central nervous system, including in the retina, hence the great importance of them for appropriate visual and cognitive development.

In this study, the investigators assessed anthropometric, visual, auditory, and psychomotor development in very preterm infants who had diets supplemented with different LCPUFA amount of AA to support the importance of sufficient AA values in formula.

Study Overview

Detailed Description

the investigators carried out a prospective randomized controlled double blinded trial in order to study nutritional supplements for preterm infants <1500 grams and/or <32 weeks gestational age (GA) who were born in clinical University Hospital of Santiago de Compostela (CHUS). They were enrolled for a period of 14 months (from July 2011 to August 2012) and followed up from birth until 2 years of age. Milk formulas were provided either as adjunct to insufficient amount of breast milk, or as full formula feeding. Breastfeeding was actively encouraged. Patients were randomized into one of the two formula groups, depending on the type of formula they were to receive. Group A's formula was supplemented with DHA (0.3% of all fatty acids) and AA (0.6%) with an ω-6/ω-3 ratio of 2/1. Group B's formula was supplemented with DHA (0.3%) and AA (0.3%) with an ω-6/ω-3 ratio of 1/1.

Primary outcome:

Assessment of psychomotor development with the Brunet Lézine scale at 2 years of age (Early Care Unit CHUS)

Secondary outcomes:

Physical examination and anthropometric measurements (weight, length, and head circumference) at birth and at 3, 6, 9, 12, 18, and 24 months of age (Neonatology Unit CHUS) Blood levels of fatty acids in the first week of life and at 3 months, 6 months, and 12 months. (Metabolic Unit. Hospital de Cruces, Bilbao) Visual- and auditory-evoked potentials at 6 and 12 months of age (Neurophysiology Unit CHUS)

Study Type

Interventional

Enrollment (Actual)

45

Phase

  • Phase 2

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 minute to 2 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Living infants who were less than 1500 grams and/or less than 32 weeks gestational age, and whose parents accepted and subscribed the informed consent

Exclusion Criteria:

  • Preterm infants with any severe malformation.
  • Extremely preterm infants with a gestational age of less than 25 weeks.
  • Infants whose parents could not complete the follow-up process in our study center.
  • Preterm infants with severe intraventricular hemorrhage or periventricular leukomalacia (more than grade 2).
  • Neonates who did not need supplementary milk nutrition, i.e. breastfed-only children.

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: Screening
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Group A
Preterm infants formula A Pretarm infants were fed on formula with Arachidonic acid (0.6%) and Docosahexaenoic acid (0.3%)
Group A will receive a preterm infants formula supplemented with AA (0.6%) and DHA (0.3%) until they have three months corrected age. At 3 and 6 months of corrected age, we changed the type of milk according to the nutritional requirements, but maintained the same ratio of AA and DHA (2/1) until one year corrected age.
Active Comparator: Group B
Preterm infants formula B Pretarm infants were fed on formula with Arachidonic acid (0.3%) and Docosahexaenoic acid (0.3%)

Group B will receive other Preterm infants formula very similar, but with AA (0.3%) and DHA (0.3%) also until they have three months corrected age.

At 3 and 6 months of corrected age, we changed the type of milk according to the nutritional requirements, but maintained the same ratio of AA and DHA (1/1) until one year corrected age.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychomotor development
Time Frame: From september 2013 to november 2014 (at two years of corrected age)
Evaluation of psychomotor development by making Brunet-Lezine scale at 2 years of corrected age.
From september 2013 to november 2014 (at two years of corrected age)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Levels of fatty acids in plasma
Time Frame: From october 2011 to november 2013 (from 3 months to 1 years old)
Blood samples were obtained from study children to study the levels of fatty acids in plasma at 3 , 6 and 12 months of life
From october 2011 to november 2013 (from 3 months to 1 years old)
Visual- and auditory-evoked potentials
Time Frame: From january 2012 to February 2013 (from 6 months to 1 years old)
Visual- and auditory-evoked potentials were studied with special scale at 6 and 12 months of life
From january 2012 to February 2013 (from 6 months to 1 years old)
Weight
Time Frame: From october 2011 to november 2014 (from 6 months to 2 years old)
Weight at 3, 6, 9, 12, 18, and 24 months of life
From october 2011 to november 2014 (from 6 months to 2 years old)
Length
Time Frame: From october 2011 to november 2014 (from 6 months to 2 years old)
Length at 3, 6, 9, 12, 18, and 24 months of life
From october 2011 to november 2014 (from 6 months to 2 years old)
Head circumference
Time Frame: From october 2011 to november 2014 (from 6 months to 2 years old)
Head circumference at 3, 6, 9, 12, 18, and 24 months of life
From october 2011 to november 2014 (from 6 months to 2 years old)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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.

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

July 1, 2011

Primary Completion (Actual)

November 1, 2014

Study Completion (Actual)

March 1, 2015

Study Registration Dates

First Submitted

July 14, 2015

First Submitted That Met QC Criteria

July 17, 2015

First Posted (Estimate)

July 20, 2015

Study Record Updates

Last Update Posted (Estimate)

July 20, 2015

Last Update Submitted That Met QC Criteria

July 17, 2015

Last Verified

July 1, 2015

More Information

Terms related to this study

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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