Outpatient Birth: Pilot Study

Not Applicable

Completed

• Conditions: Outpatient Birth

• Registration Number: NCT03815227
• Lead Sponsor: Centre Hospitalier Régional Metz-Thionville

Brief Summary

The diminution of the average length stay (ALS) in French maternity is a clear evolution, the objective of the draft law on social security is to reduce the ALS to equal other OECD countries. The over-medicalization of maternal health raises the question of relevant and iatrogeny of Professional practices. Furthermore, pregnant woman, future parents expressed their wish for an individual support and more physiological respectful. A more-effective Professional coordination is expected where the midwife is a major player.

Detailed Description

The aim of the study is to identify and evaluate an outpatient birth path during the first 24 hours after the birth.

Study Timeline

• Study First Submitted: 2019-01-23
• Study First Submitted QC: 2019-01-23
• Study First Posted: 2019-01-24
• Study Start: 2019-01-31
• Primary Completion: 2021-06-30
• Study Completion: 2021-09-27
• Status Verified: 2022-05
• Last Update Submitted: 2022-05-05
• Last Update Posted: 2022-05-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

• With no multiple pregnancy, of less than 20 weeks of gestation
• With a BMI between 17,5 and 35 kg/m²
• is able to understand research's informations
• affiliated member of the social security system
• Have given an informed consent

Exclusion Criteria

• With psychological vulnerability, social vulnerability, addictions and high dependency
• With an unbalanced chronic pathology or susceptible to contraindicated a physiologic birth
• With history of caesarean, foeto-maternal incompatibility, gestational hypertension, pre-eclampsia, HELLP syndrome or retro-placental hematoma, sphincter tear
• With history of birth with perinatal asphyxia and sequelae or an unexplained perinatal death
• With history of puerperal psychosis
• Under guardianship

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Output rate	Day 1	Output rate within 24 hours of birth

Trial Locations

Locations (1)

CHR Metz Thionville; 🇫🇷 Thionville, Moselle, France