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Recruiting NCT06844019

Birth & Breastfeeding Support Study

Observational Breastfeeding Breastfeeding Initiation Breastfeeding Duration Birth

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Breastfeeding, Breastfeeding Initiation, Breastfeeding Duration, Birth. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this observational study is to learn about the effects of birth practices such as cesarean section and vacuum assisted birth and diseases such as gestational diabetes and preeclampsia on exclusive breastfeeding. The main question it aims to answer is: • Does cesarean section, vacuum assisted birth, gestational diabetes and preeclampsia affect exclusive breastfeeding three months after birth? Participants answer eight online survey questions. One survey is distributed before birth and the remaining seven surveys are distributed after birth at three, seven and four-teen days, as well as one, three, six and twelve months after birth.

Primary outcome measures

  • Exclusive Breastfeeding [Time frame: 3 months]

Eligibility criteria

Inclusion Criteria: 18 years, intention to breastfeed, single gestation, reads and understands Danish -

Exclusion Criteria: Twin gestation, less than 18 years, no intention to breastfeed, does not read and understand Danish

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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Denmark · 1 center
  • Herlev & Gentofte University Hospital — Herlev

Identifiers

NCT: NCT06844019 · F-24074649

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗