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Clinical Trials in Canada / NCT01623934
Active, not recruiting Observational

Role of Adipokines in Glucose Regulation During Pregnancy and in Fetal Development

NCT01623934 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2010-01
Last updated
2024-10-18

Condition(s) studied

Gestational DiabetesInsulin ResistanceObesity Prevention

Study summary

This study includes 2 phases. During phase 1, pregnant women are followed over the course of pregnancy. The phase 2 is a follow-up of the mother-child dyad at 3, 5 and 10-12 year after delivery.

The purpose of this phase 1 is to :

* assess the contribution and interactions of adipokines in the development of insulin resistance during pregnancy and gestational diabetes;
* assess levels of maternal adipokines as determinants of development and fetal growth;
* determine the genetic variations that influence levels of adipokines and glucose regulation during pregnancy and in newborns.

The purpose of this phase 2 is to:

* identify DNA methylation variations at birth that are predictive of childhood overweight/obesity.
* identify maternal characteristics associated with DNA methylation variations predictive of childhood overweight/obesity.
* establish whether the loci predictive of childhood overweight/obesity at birth are still differentially methylated at 5 years of age (samples collected at 5 years of age).
* identify DNA methylation variations at birth that are predictive of childhood neurodevelopment problems at 3, 5 and 10 years of age.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * age ≥ 18 yrs * gestational age between 6 and 13 weeks from last menstrual period * no recognized diabetes or drugs interfering with glucose metabolism * alcohol \< 2 drinks/day * not involved in regular high intensity physical activity * otherwise good health status Exclusion Criteria: * twin pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre de recherche du Centre hospitalier universitaire de Sherbrooke Sherbrooke Quebec

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01623934 on ClinicalTrials.gov ↗ ← All trials in Canada