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Can a video call replace your Pre-Birth anesthesia check?

NCT ID NCT05975411

Knowledge-focused Sponsor: University Hospital, Caen 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether pregnant women can have their pre-birth anesthesia consultation through a video call instead of coming to the hospital. 60 women participated, using a telemedicine cabin or cart near their home. The goal was to see if the video assessment of the airway is as good as an in-person check, and to gather feedback from patients and doctors.

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.

Participants

60 people

The number who actually took part.

Started

Jan 2021

Finished

Dec 2021

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.

Who is studied

pregnancy women

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: * Pregnant woman * over 18 years old * beneficiary of social security/CMU * Non-emergency pre-anesthesia consultation * delivery planned at the maternity ward of the University Hospital of Caen * living in the vicinity of Dozulé or living near an establishment with a telemedicine cart equipped with the necessary equipment * Having received clear and honest information about the study, and having given their consent * Having given their consent for a telemedicine consultation * patient without comorbidity Exclusion Criteria: * Patient refusal * Patient under guardianship * Patient with psychomotor disability; hearing impaired; visually impaired * Difficulties in understanding information, expression; foreign language * Pathological pregnancy

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Conditions

The condition(s) this trial relates to.

pregnancy disorder

As listed by the trial registrant

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

Pregnancy related

Contacts and locations

Locations

  • CAEN University Hospital

    Caen, France

More trials for these conditions

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