Clinical Trials Directory

Trials / Completed

CompletedNCT04897451

Quality of Life After Cervical Ripening

Quality of Life 3 Months After Cervical Ripening

Status
Completed
Phase
Study type
Observational
Enrollment
160 (actual)
Sponsor
Centre Hospitalier Departemental Vendee · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Women's experience of childbirth differs with type of labor, mode of delivery and parity. Induction of labor (IOL) is associated with lower satisfaction of women than spontaneous labor. 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.

Conditions

Interventions

TypeNameDescription
OTHERQuestionnaireEQ5D-5L questionnaire self-reported 3 months after delivery

Timeline

Start date
2021-07-08
Primary completion
2021-12-12
Completion
2021-12-12
First posted
2021-05-21
Last updated
2022-09-28

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04897451. Inclusion in this directory is not an endorsement.