Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Sugar drinks during labor may cut need for forceps delivery

NCT ID NCT01022697

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

4,142 people

The number who actually took part.

Start date

Jan 2008

Finished

Jul 2012

Lead sponsor

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

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Childbirth are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Centre Hospitalier

    Bayeux, 14400, France

  • Centre Hospitalier Mémorial France Etats-Unis

    Saint-Lô, 50000, France

  • Centre Hospitalier du Rouvray

    Elbeuf, 76350, France

  • Clinique du Parc

    Caen, 14000, France

  • Hospital, Avranches

    Avranches, France

  • Hospital, Mont Saint Aignan

    Mont-Saint-Aignan, France

  • University Hospital, Caen

    Caen, 14033, France

  • University Hospital, Lille

    Lille, France

  • University Hospital, Rouen

    Rouen, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.