Actively Recruiting

Phase Not Applicable
Age: 14Days - 14Days
All Genders
Healthy Volunteers
NCT06624709

The Benefit in Terms of Improvement in Haemoglobin Level at 6 Months in Premature Babies Receiving Alternate Iron Substitution 4 Times a Week Compared to a Daily Substitution

Led by Riccardo Pfister · Updated on 2025-05-25

160

Participants Needed

2

Research Sites

130 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

BienFer is a double-blinded randomized controlled trial about iron substitution and abdominal pain. Premature babies and low birth weight babies have lower iron stores than term newborns and are therefore at greater risk of iron deficiency and anemia. Iron deficiency could have consequences for cerebral development. Ferric substitution reduces the risk of iron deficiency and anemia. It is common to replace premature babies with iron substitution between 2 weeks and 6 months of life. In practice, the medical staff notice that newborn with iron substitution have abdominal pain and constipation. A study in the adult population shows that alternate iron supplementation versus daily supplementation improved iron absorption, with no difference in hemoglobin level and decrease abdominal pain. Studies in children shows that intermittent iron supplementation do not change hemoglobin and ferritin level and improve adherence. There is no data comparing daily versus alternate supplementation in premature babies. The aim of the study is to evaluate if alternate (4 times/week) iron supplementation is equivalent to daily iron substitution for hemoglobin values in premature babies between 28 0/7 weeks amenorrhea (WA) and 34 6/7 WA, and if it reduces abdominal discomfort and inflammation, and if it improves compliance.

CONDITIONS

Official Title

The Benefit in Terms of Improvement in Haemoglobin Level at 6 Months in Premature Babies Receiving Alternate Iron Substitution 4 Times a Week Compared to a Daily Substitution

Who Can Participate

Age: 14Days - 14Days
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Premature babies between 28 0/7 weeks and 34 6/7 weeks of gestation
  • Parental consent given after birth
  • Age of 2 weeks at start of study
Not Eligible

You will not qualify if you...

  • Anemia with hemoglobin less than 80 g/L at 2 weeks of age
  • Intraventricular Hemorrhage stage III or IV
  • Necrotizing Enterocolitis
  • Enteral feeding less than 100 ml/kg/day after 2 weeks of life
  • Congenital disorder

AI-Screening

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Trial Site Locations

Total: 2 locations

1

HUG

Geneva, Canton of Geneva, Switzerland, 1211

Actively Recruiting

2

CHUV

Lausanne, Canton of Vaud, Switzerland, 1011

Actively Recruiting

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Research Team

C

Céline Ferraz

CONTACT

R

Riccardo E Pfister, MD, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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