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Should we restrict food intake during labor?

Should we restrict food intake during labor? A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11794106
Enrollment
116
Registered
2023-12-02
Start date
2018-12-18
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Food intake during labor Pregnancy and Childbirth

Interventions

All patients were allowed to consume water or clear fluids before entering the labor room and having epidural anesthesia. After signing an informed consent, patients were randomized for oral food inta

Sponsors

Meir Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Singleton, term gestation (=37 weeks) during the end of the latent phase of the early second phase of labor, based on regular painful contractions and cervical examination. To decrease the risk of general anesthesia, which is a known risk factor for aspiration, the researchers recruited patients after receipt of epidural anesthesia.

Exclusion criteria

Exclusion criteria: 1. Women with pregestational or gestational diabetes 2. Multiple gestations 3. Non-reassuring fetal heart rate prior to randomization

Design outcomes

Primary

MeasureTime frame
A composite outcome of complications attributed to eating during labor and delivery. The researchers included emergent cesarean section, assisted vaginal deliveries and other indications for interventions that might need a general anesthesia with a potential risk of aspiration and chemical pneumonia such as uterine revision or manual lysis of retained placenta and advanced vaginal lacerations, general anesthesia, postpartum fever, aspiration and prolonged postpartum hospitalization of 5 days and more attributed to complications of aspiration measured using patient records at the end of the study.

Secondary

MeasureTime frame
Oxytocin augmentation during labor, second stage duration, need for analgesia, emergent cesarean section, early maternal and neonatal outcomes, aspiration and chemical requirements measured using patient records at the end of the study.

Countries

Israel

Contacts

Public ContactGil Shechter Maor
gil.shechter@clalit.org.il+972 97472210

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 6, 2026