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Obesity's secret impact on labor revealed in new study

NCT ID NCT01762683

Knowledge-focused Sponsor: Centre Hospitalier Universitaire Dijon Source: ClinicalTrials.gov ↗

What the study statuses mean

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study looked at how obesity might affect the cells in the uterus that help with labor. Researchers took blood and uterine tissue samples from 38 women having C-sections, some with normal weight and some obese. They wanted to see if certain cells and chemicals in the blood could change how uterine cells behave, which might explain why obese women sometimes have delivery problems.

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

38 people

The number who actually took part.

Started

Apr 2012

Finished

Jan 2016

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: * Informed consent signed * Patient affiliated with a social security scheme * In front of for obstetrical reasons to give birth by caesarean section (scheduled caesarean section) * Or a woman who is not obese in labour and needs to undergo a cesarean section * No obvious infectious context * Age \> 18 years old Exclusion Criteria: * Obvious inflammatory or autoimmune diseases * Suspected or confirmed infectious context, including virale infection VIH, VHC, VHB * Coagulation disorders

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Conditions

The condition(s) this trial relates to.

Obesity pregnancy disorder

As listed by the trial registrant

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

Pregnancy complication

Contacts and locations

Locations

  • Clinique Sainte Marthe

    Dijon, 21000, France

  • Maternité du CHU de Dijon

    Dijon, Bourgogne-Franche-Comté, 21000, France

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