CClinicalTrials.gg
CompletedNCT05975411CATmedOUpdated Mar 10, 2026

Telemedicine Anesthesia Consultation, Pilot Study in Obstetrics.

An observational study in Pregnancy Related, sponsored by University Hospital, Caen. Completed at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-10.

Sponsored by University Hospital, Caen · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
18 Years and older
Sex
Female
01

Study summary

Pilot study in Lower Normandy concerning a total of 90 patients scheduled for a pre-anaesthesia consultation in obstetrics. These parturients who plan to give birth at the maternity hospital of the CHU will be invited to carry out their anesthesia consultation with a view to childbirth either by way of the telemedicine cabin installed in Dozulé, or by way of the telemedicine trolley installed in a center close to their place of residence, or at the CHU de Caen as usual.

The validation of the adequacy of the possibilities of telemedicine with the requirements of the anesthesia consultation worked upstream is the main objective of this work, the appreciation of the parturient at this consultation, the appreciation of the consulting and validating professionals will also be collected with the aim of a maximum optimization of this new offer intended for the region.

02

Conditions studied

  • Pregnancy Related
03

In context

Lead sponsor

University Hospital, Caen is the lead sponsor of 505 studies on the registry; 80 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

pregnancy women

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

Exclusion Criteria:

  • Patient refusal
  • Patient under guardianship
  • Patient with psychomotor disability; hearing impaired; visually impaired
  • Difficulties in understanding information, expression; foreign language
  • Pathological pregnancy
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (actual)
Patient registry
No

Groups and cohorts

  • telemedecine cabin

    Anesthesia Consultation with telemedicine cabin installed in Dozulé

    Other: Anesthesia Consultation with telemedicine

  • telemedicine trolley

    Anesthesia Consultation with telemedicine by way of the telemedicine trolley installed in a center close to their place of residence

    Other: Anesthesia Consultation with telemedicine

  • standard

    Anesthesia Consultation at the CHU de Caen as usual.

Interventions

  • OtherAnesthesia Consultation with telemedicine

    Anesthesia Consultation with telemedicine

06

What researchers measure

Primary outcomes

  1. assessment of the airways via a telemedicine device

    * Composite score (rated from 5 to 14) evaluating the risk of difficult orotracheal intubation which is based on the five main elements of the airway evaluation during the anesthesia consultation which are: * Mouth opening * Mallampati score * Cervical spine mobility * Thyro-chin distance * Patient Profile * Lip test

    Time frame: baseline

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Study locations

1 site
  • CAEN University Hospital
    Caen, France
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05975411
Lead sponsor
University Hospital, Caen
Responsible party
Sponsor
First posted
Aug 3, 2023
Start date
Jan 11, 2021
Primary completion
Mar 15, 2021
Completion
Dec 31, 2021
Last update
Mar 10, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.

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