Comparison of Antrum Surface Between Women With Operative Hysteroscopy or Planned Caesarean Section

NCT ID: NCT03776565

Last Updated: 2020-01-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

137 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-11-26

Study Completion Date

2019-11-27

Brief Summary

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Realization of a gastric ultrasound just before surgery, to measure the surface of antrum of stomach and compare if divergence sizes can be observed between women with a operative hysteroscopy and women with a planned caesarean section. To know if anaesthesia need to be adapted to the population.

Detailed Description

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Conditions

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Pregnancy Related

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Operative hysteroscopy

women with an operative hysteroscopy planned

Ultrasound

Intervention Type OTHER

Ultrasound of antrum of stomach

Planned caesarean section

Pregnant women with a planned caesarean section

Ultrasound

Intervention Type OTHER

Ultrasound of antrum of stomach

Interventions

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Ultrasound

Ultrasound of antrum of stomach

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age between 18 and 40
* Membership of a national insurance scheme
* Written consent
* Physical status score or American Society of Anesthesiologists (ASA) score = 1 or 2
* Planned caesarean section or operative hysteroscopy

Exclusion Criteria

* Not able to give her written consent (not speaking French), under legal protection
* Insulin-dependant diabetes
* Hiatus hernia
* History of gastro-oesophageal surgery
* Contraindication to right lateral decubitus
* Treatments with anti-acids before ultrasounds.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hopital Foch

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Frederic Mercier, MD PhD

Role: STUDY_DIRECTOR

Hopital Beclere (APHP)

Locations

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Hopital Béclère (APHP)

Clamart, , France

Site Status

Hopital Foch

Suresnes, , France

Site Status

Countries

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France

Other Identifiers

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2017029F

Identifier Type: -

Identifier Source: org_study_id

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