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Sugar drinks during labor may cut need for forceps delivery
NCT ID NCT01022697
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether giving women glucose drinks every 3 hours during labor could reduce the need for assisted delivery (forceps or vacuum) and shorten labor. Over 4000 women participated. The idea is that childbirth is like a sports event requiring energy, and oral glucose might help without the risks of intravenous sugar. The main goal was to see if fewer women needed instruments to deliver their baby.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- glucose drink
- What this could lead to
- If effective, glucose drinks could become a simple, low-cost way to reduce the need for forceps or vacuum during childbirth and shorten labor.
- What could go wrong
- This is a completed study, but earlier small studies found no clear benefit. The results may not show a meaningful reduction in assisted deliveries or could have limitations in generalizing to all birthing people.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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4,142 people
The number who actually took part.
- Start date
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Jan 2008
- Finished
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Jul 2012
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age \>= 18 yrs * Entering for childbirth * Informed written consent Exclusion Criteria: * more of 8 cm of dilatation * Caesarean section planned * natural delivery non-indicated * pre-partum hemostasis troubles * salicylic acid or anticoagulant treatment * pre-eclampsia or HELLP syndrome * diabetic neuropsy with troubles in gastric emptying * IMC \> 40 at the end of pregnancy * understanding of the information * under guardianship
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre Hospitalier
Bayeux, 14400, France
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Centre Hospitalier Mémorial France Etats-Unis
Saint-Lô, 50000, France
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Centre Hospitalier du Rouvray
Elbeuf, 76350, France
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Clinique du Parc
Caen, 14000, France
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Hospital, Avranches
Avranches, France
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Hospital, Mont Saint Aignan
Mont-Saint-Aignan, France
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University Hospital, Caen
Caen, 14033, France
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University Hospital, Lille
Lille, France
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University Hospital, Rouen
Rouen, France
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