Study Results
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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COMPLETED
160 participants
OBSERVATIONAL
2021-07-08
2021-12-12
Brief Summary
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A Nigerian study of 252 women with induced labor, irrespective of parity and device used for IOL and a French cohort study of 3042 women with IOL have been published. Theses latter identified several determinants of maternal dissatisfaction.
However, no published study has reported the assessment of quality of life of women at long term after cervical ripening according to the device required for cervical ripening.
The aim of this study is to characterize the quality of life of women after cervical ripening according to parity and device required, and to assess possible factors associated with this quality of life at long-term after delivery.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Women with cervical ripening in the context of artificial labor induction
Questionnaire
EQ5D-5L questionnaire self-reported 3 months after delivery
Interventions
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Questionnaire
EQ5D-5L questionnaire self-reported 3 months after delivery
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Centre Hospitalier Departemental Vendee
OTHER
Responsible Party
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Principal Investigators
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Guillaume DUCARME
Role: PRINCIPAL_INVESTIGATOR
CHD Vendee
Locations
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CHD Vendée
La Roche-sur-Yon, , France
Countries
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Other Identifiers
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CHD21-0028
Identifier Type: -
Identifier Source: org_study_id
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