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A Trial Comparing Two Breast Pumps in Mothers Expressing Milk for Their Preterm Infants

I

Institute of Child Health

Status

Unknown

Conditions

Milk Production

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This is a randomised controlled trial investigating the performance of two, 'state of the art' electric breast pumps in mothers who have delivered preterm infants. The main data collection period will be up to day 10 post delivery data. Data collected will include a record of the weight of milk produced during the first 10 days and a short questionnaire to find the mothers' opinions of the pumps used. On Day 5 a timed and weighed expression of 15 minutes will be carried out. After the first 10 days, mothers will be asked to collect brief information on their continuing use of their pumps and subsequent duration of breast and bottle feeding, mothers will be contacted at 3 and 6 months post-term

Enrollment

176 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Mothers who have delivered, preterm (before 34 weeks) infants who plan to express breast milk for their infant(s). Their infants will need to be less than 72 hours old prior to enrolment and likely to remain in NICUs for at least 10 days.

Exclusion criteria

  • Other mothers not fitting inclusion criteria.

Trial design

176 participants in 2 patient groups

Electric Pump 1 (ISIS Duo iQ Electric Breast Pump)
Description:
This is a parallel trial where subjects (mother of preterm infants) will be allocated to use one of two electric breast pumps to express milk. The use of electric breast pumps is routine practice on neonatal units in the UK.
Electric Pump 2 (Medela Symphony Electric Breast Pump)
Description:
This is a parallel trial where subjects (mother of preterm infants) will be allocated to use one of two electric breast pumps to express milk. The use of electric breast pumps is routine practice on neonatal units in the UK.

Trial contacts and locations

1

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Central trial contact

Pat Burton

Data sourced from clinicaltrials.gov

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