Lactation; Insufficient, Partial

2

Review clinical trials related to Lactation; Insufficient, Partial. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Comparing Integrative Midwife-led vs. Fragmented Inpatient Postpartum Care: Impact on Satisfaction and Transition to Motherhood

The goal of this clinical trial is to compare two different forms of postnatal care to find out which is most beneficial for mothers and their children after birth and with which they are most satisfied. One is a nurse-led, seperate model of care and the other is a midwife-led, integrative model of care. Participants are healthy women between the ages of 18 and 50. They gave birth between 36+0 and 42+0 weeks of pregnancy and had a child. The type of birth is not an inclusion or exclusion criteria. Our hypotheses are: i) that maternal satisfaction with care in a midwife-led, integrative care model is higher than in separate maternal and infant care; ii) that a positive postpartum experience leads to earlier and increased maternity competence; iii) that a higher breastfeeding rate at the time of the survey in the fourth month can be achieved through integrative care. Participants will be randomly assigned, after birth of their child, to either the group cared for by a nurse or the group cared for by a midwife.

Participants needed: 784
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Medical University of ViennaUpdated: Jul 22, 2025Locations: 1
Eligibility criteria

Women aged 18 to 50 years at the time of delivery [+5]

Women younger than 18 or older than 50 at the time of delivery [+3]

Status: Recruiting

Sodium Awareness in Lactation Trial

SALT is a multi-centre, non-blinded, non-randomized prospective interventional pilot study teaching lactating parents of hospitalized preterm infants how to test their breastmilk sodium (Na) using point-of-care (POC) meters. A drop in Na is a sign of secretory activation in the breast that is associated with adequate short and long-term breast milk volumes in this vulnerable population. Primary Objective: Establish feasibility, acceptance, and time cost of parent-led parent milk Na testing in the first 14 days postpartum Secondary Objective: Further investigate relationships between pumping behaviours, lactation risk factors, daily milk Na and lactation outcomes Exploratory Objective: Explore how POC Na data may be used to modify pumping behaviour and milk volumes

Participants needed: 40
Trial details
Biological sex: FemaleType: InterventionalSponsor: The Hospital for Sick ChildrenUpdated: May 28, 2025Locations: 2
Eligibility criteria

Consent provided [+4]

Potential study participant's infant is critically ill and not expected to survi... [+6]