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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03283579
Other study ID # mlopez
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 2003
Est. completion date December 2015

Study information

Verified date September 2017
Source Barcelona Institute for Global Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aimed to evaluate the longitudinal association between n-6:n-3 LCPUFAs ratio in cord blood and child ADHD symptoms at 4 and 7 years old. This study was based on the INMA project, a population-based birth cohort in Spain. Higher cord blood n-6:n-3 ratio was associated with higher subclinical ADHD symptoms during early and mid-childhood.


Recruitment information / eligibility

Status Completed
Enrollment 2644
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion criteria:

- Age 16 years or older

- Singleton pregnancy

- No use of assisted reproductive techniques

- Intention to deliver at the reference hospital

- Ability to speak and understand Spanish or a local language

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Barcelona Institute for Global Health

Outcome

Type Measure Description Time frame Safety issue
Primary Fatty acid ratio in cord blood 2004-2008
Primary ADHD 4 years old 2008-2012
Primary ADHD 7 years old 2012-2016
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