Actively Recruiting
Impact of Prepartum Intravenous Fluid Intake on Newborn Weight Loss in the First Days of Life
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2025-11-21
200
Participants Needed
1
Research Sites
35 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
At birth, the infant's weight was measured daily to assess the adequacy of nutritional intake. This indicator can be influenced by various factors related to the mother, her pregnancy, as well as medical interventions during the pre-delivery phase, such as pre-partum maternal fluid intakes, and the subsequent feeding method chosen for the newborn infant. This study aimed at exploring the association between maternal vascular fluid loading during labor in the pre-partum period and neonatal weight loss in the first two days of life. The study focuses on infants fedded with infant formula. This observational, retrospective, single-center study was carried out at the Amiens University Hospital Center. The participants were mothers aged 18 and older, hospitalized in the maternity ward following full-term delivery (\> 37 weeks of gestation). Data were collected through the medical records of the patient and their newborn. The investigators hypothesize that a relationship may exist between maternal pre-partum vascular fluid loading and neonatal weight loss in the first two days of life, in infants fed with infant formula. These results could raise awareness and help adapt medical and parental approaches to neonatal weight loss.
CONDITIONS
Official Title
Impact of Prepartum Intravenous Fluid Intake on Newborn Weight Loss in the First Days of Life
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Full-term delivery (≥37+0 weeks of gestation)
- Singleton pregnancy
- Mother aged 18 years or older
- Infant fed exclusively with infant formula in the maternity ward for the first 2 days
You will not qualify if you...
- Mother under guardianship
- Mother does not understand French
- Mother objects to use of her personal data for research
- Incomplete or incorrect medical records
- Mixed or exclusive breastfeeding
- Mother had hemodynamic disorder requiring fluid filling within 12 hours before delivery
- Baby has kidney disease or urinary tract problems
- Baby has cleft lip, palate, or labio-palate
AI-Screening
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Trial Site Locations
Total: 1 location
1
CHU Amiens Picardie
Amiens, Picardie, France, 80054
Actively Recruiting
Research Team
P
Pierre Tourneux, Pr
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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