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Fluid injection before second Baby-Turn attempt shows promise

NCT ID NCT00465712

Disease control Sponsor: University Hospital, Tours Source: ClinicalTrials.gov ↗

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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether injecting fluid around the baby (amnioinfusion) before a second attempt to turn a breech baby head-down makes the turning more successful. It included 119 pregnant women with a single baby in breech position at full term whose first turning attempt failed. The study was stopped early, and the main goal was to see how many babies were head-down at birth.

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

119 people

The number who actually took part.

Start date

Jul 2006

Finished

May 2011

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

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * single fetal pregnancy * breech presentation * at term * initial failure of external cephalic version * structurally normal foetus Exclusion Criteria: * polyhydramnios * anhydramnios * abnormality of the fetal heart rhythm * uterine congenital malformation * cesarian section for a previous birth * unability to understand study

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Conditions

The condition(s) this trial relates to.

Breech Presentation

As listed by the trial registrant

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

Breech presentation

Contacts and locations

Locations

  • Mother Child University Hospital

    Nantes, 44000, France

  • Olympe de Gouges Women Health Centre, Bretonneau University Hospital

    Tours, 37000, France

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