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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01487889
Other study ID # PINGU0911DO
Secondary ID
Status Completed
Phase N/A
First received September 15, 2011
Last updated November 5, 2014
Start date April 2011
Est. completion date September 2013

Study information

Verified date November 2014
Source Research Institute of Child Nutrition, Dortmund
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Ministry of Education and Research
Study type Interventional

Clinical Trial Summary

Primary objective of this study is to examine the effects of 2 different approaches of dietary strategies to optimise fatty acid composition in complementary food on infant's fatty acid status and its consequences on cognitive and visual development.

Subjects are randomly assigned to one of three groups:

- Rapeseed oil (high in n-3 PUFA and small n-6:n-3 ratio to support endogenous n- 3 LC-PUFA metabolism)

- Fatty fish (preformed n-3 LC-PUFA, especially DHA)

- Corn oil (as control group, high in n-6 PUFA, common in complementary food).

The intervention starts with the beginning of complementary feeding as generally recommended between 4 to 6 months of age and ends at the age of 10 months. For this period of time subjects of all groups receive commercial vegetable-potato-meat-meals as part of complementary food which only differs in the fatty acid composition.


Description:

A well balanced supply of polyunsaturated fatty acids, in particular the omega-3 long chain docosahexaenoic acid (DHA), in early childhood is essential for children's cognitive and visual development. DHA can either be supplied preformed in the diet (e.g. via fatty fish) or synthesised by conversion of its essential precursor alpha-linolenic acid (e.g. via rapeseed oil). The study examines the effect of two different approaches to optimise infants´ fatty acid status.

The study sample consists of healthy newborns and their mothers (3 x 57 infants according to a priori power calculation) who are enrolled in delivery hospitals in the region of Dortmund, Germany. In total, the individual study program covers the first 10 months of infant's life. Biomarkers of fatty acid status from the mother are collected 8 weeks pp for the estimation of pre- and perinatal fatty acid supply. Additionally, information on maternal diet during pregnancy and after delivery is assessed. The intervention covers the period of complementary feeding (from 4 to 6 months of age until 10 months of age). In all groups the specific study food is given 5 to 7 times a week, whereas 2 of these are fish meals in the fatty fish group. At the age of 4 and 10 months blood samples are collected from the infants to examine the effect on blood fatty acid status. Parameters of visual and cognitive development are also assessed at the age of 4 and 10 months using VEP examinations and Bayley scales. Infants´ dietary intake is assessed from the end of the 2 months until 10 months of age using continuous weighed dietary records.


Recruitment information / eligibility

Status Completed
Enrollment 214
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A to 8 Weeks
Eligibility Inclusion Criteria:

- a term healthy newborn infant ( birth weight > 2500 g, gestational age > 37 weeks

- German speaking mother

- the intention of the mother to breast-feed the children and to feed study menus at least 5 times per week beginning in the fifth to seventh month of life.

Exclusion Criteria:

- preterm children

- twins

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Fatty acid composition of complementary food
Groups receive commercial vegetable-potato-meat-meals as part of complementary food which differs in the fatty acid composition

Locations

Country Name City State
Germany Research Institute of Child Nutrition Dortmund

Sponsors (4)

Lead Sponsor Collaborator
Research Institute of Child Nutrition, Dortmund Dr. von Hauner Children's Hospital, Germany, Pediatric Clinic Dortmund, Germany, University of Potsdam

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Infants´ fatty acid status Fatty acids (saturated fatty acids, monounsaturated fatty acids, polyunsaturated fatty acids including long-chain polyunsaturated fatty acids) are measured in percent of total fatty acids in erythrocyte membranes, whole plasma, and cheek cells in order to assess the fatty acid composition. 10 months after delivery No
Secondary Infants´ visual development Infants´ visual development is assessed using the visual evoked potentials method. 10 months after delivery No
Secondary Infants´ cognitive development Infants´ cognitive development is assessed using the Bayley II scale. 10 months after delivery No
Secondary Infants´ haemogram 10 months after delivery No
Secondary Infants´antioxidant status 10 months after delivery No
Secondary Infants´ body weight 10 months after delivery No
Secondary Infants´ dietary intake from 2 until 10 months after delivery No
Secondary Maternal dietary intake pregnancy and first 2 months post partum No
Secondary Infant's preference for fish 10 month after delivery No
Secondary Infant's preference for new flavour 10 month after delivery No
Secondary Parental attitudes about fish and feeding strategies 10 months after delivery No
Secondary Mother´s fatty acid status Fatty acids (saturated fatty acids, monounsaturated fatty acids, polyunsaturated fatty acids including long-chain polyunsaturated fatty acids) are measured in percent of total fatty acids in erythrocyte membranes, whole plasma, cheek cells, and breast milk in order to assess the fatty acid composition. 2 months after delivery No
Secondary Infants´ body length 10 months after delivery No
Secondary Infant´s head circumference 10 months after delivery No
See also
  Status Clinical Trial Phase
Completed NCT00571948 - Modification in Complementary Food Composition to Improve the Status of Iron and Fatty Acids in Infants. N/A