Stopped: Unable to recruit to enrollment target
A randomized clinical trial (RCT) to evaluate the impact of unrestricted low fat, low residue oral intake during labor on maternal and neonatal outcomes as well as maternal satisfaction.
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Nausea
Timeframe: active labor (6cm or greater dilation) through delivery of the infant
Vomiting
Timeframe: active labor (6cm or greater dilation) through delivery of the infant
Duration of labor
Timeframe: active labor (6cm or greater dilation) through delivery of the infant
Mode of delivery
Timeframe: at birth
Aspiration
Timeframe: active labor (6cm or greater dilation) through delivery of the infant
Newborn APGAR Score
Timeframe: 5 min of life
Maternal Satisfaction
Timeframe: active labor (6cm or greater dilation) through delivery of the infant