RecruitingNCT04819893

Study of the Involvement of Fatty Acids in Retinopathy of Prematurity: Relationship Between Retinopathy of Prematurity and the Rate of Expression of Transplacental Fatty Acid Receptors.


Sponsor

Centre Hospitalier Universitaire Dijon

Enrollment

135 participants

Start Date

Apr 20, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

The development of the retinal vascular network is completed during the third trimester of pregnancy and and the first 15 days of life of the newborn. This late maturation can be problematic in cases of preterm births and result in immature retinal vascularization, known as retinopathy of prematurity (ROP). Among the various factors influencing retinal vascular development, the tissue content of omega-3 polyunsaturated fatty acids (PUFAs) appears to be a crucial element. In a previous project, OMEGA-ROP, we showed a difference in the blood bioavailability of omega-3 PUFAs in infants born at less than 28 weeks of amenorrhea who develop ROP compared to healthy newborns with no retinopathy. This study also showed that mothers experienced variations in the blood levels of omega-3 PUFAs that were contrary to the types of variations observed in their children. This suggests a sequestration of omega-3 PUFAs in the mothers of children who will develop ROP. This new project aims to better understand the underlying molecular mechanisms by studying the expression levels of placental fatty acid receptors in relation to the development of ROP in newborns.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Data collection, a biological treatment called Maternal blood sampling, and others for people with prematurity and retinopathy. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALMaternal blood sampling

5 mL sample of venous blood on arrival at the maternity ward in accordance with standard protocols

BIOLOGICALUmbilical cord blood sampling

0.5mL sample from the umbilical cord after childbirth standard protocols

BIOLOGICALPlacenta sampling

Sampling of 3 cotyledons by cutting across the thickness of the placenta

OTHERData collection

Newborn, Maternal and Premature Retinopathy Screening Data Collection


Locations(1)

Chu Dijon Bourogne

Dijon, France

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NCT04819893


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