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
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to explore how the amount of intravenous fluids given to mothers during labor before delivery might affect newborn babies' weight loss in the first two days of life. The study focuses on infants who are fed exclusively with infant formula and considers factors related to the mother, pregnancy, and medical interventions during the pre-delivery phase. It is an observational, retrospective study conducted at a single center, the Amiens University Hospital Center, involving mothers aged 18 and older who delivered full-term singletons. The study collects data retrospectively from medical records of mothers and their newborns. It examines the relationship between maternal vascular fluid loading during labor and newborn weight loss, as well as secondary outcomes like respiratory distress and jaundice in the first two days after birth. No treatments or interventions are administered by the researchers as this is an observational study. Participants' involvement includes reviewing existing medical records from the maternity ward during the first two days after birth, focusing on infants exclusively fed with infant formula. Researchers measure newborn weight loss as the primary outcome and assess correlations with maternal fluid intake and newborn health issues such as respiratory distress and jaundice. The study runs until November 2025, and all data is collected without additional procedures or interventions for participants.
CONDITIONS
Brief 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 weeks or more)
- Singleton pregnancy
- Mother aged 18 years or older
- Infant fed exclusively with infant formula during the first 2 days in the maternity ward
You will not qualify if you...
- Mother under guardianship
- Mother who does not understand French
- Mother objecting to personal data use for research
- Incomplete or incorrect medical records
- Mixed or exclusive breastfeeding
- Mother with hemodynamic disorder needing specific fluid filling within 12 hours before delivery
- Child with renal pathology or uropathy
- Child with cleft lip, palate, or labio-palate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 days
Participants who undergo routine care are observed to assess the correlation between maternal fluid intake before delivery and newborn weight loss, respiratory distress, and jaundice during the first 2 days of life.
1 to 2 visits during the first 2 days after delivery
Trial Site Locations
Total: 1 location
1
CHU Amiens Picardie
Amiens, Picardie, France, 80054
Actively Recruiting
Research Team
P
Pierre Tourneux, Pr
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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