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The Fluid In Low risk Labour Trial

The effect of conservative versus routine intrapartum fluid management in women with epidural analgesia on breastfed newborn weight loss: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN06221064
Enrollment
200
Registered
2008-09-29
Start date
2008-10-15
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fluid management in labour Pregnancy and Childbirth

Interventions

Total duration of treatment is from the time of admission to the labour unit until the time of delivery. Patients will be randomised to one of the following fluid management techniques: Usual Intrapa

Sponsors

Sunnybrook Health Sciences Centre (Canada)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women in early labour, 19 - 40 years of age 2. Experiencing a labour at no identified risk 3. Anticipating a vaginal birth 4. Planning to breastfeed 5. Requesting an epidural

Exclusion criteria

Exclusion criteria: 1. Planning discharge before 48 hours 2. Unable to read and write English 3. Previous breast surgery 4. Expected to deliver in the next 4 - 5 hours

Design outcomes

Primary

MeasureTime frame
Breastfed newborn weight loss in the first 48 hours.

Secondary

MeasureTime frame
Breastfeeding exclusivity, measured prior to discharge from the postpartum unit.

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026