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Quality of Life After Cervical Ripening (MATUCOL-QOL)

C

Centre Hospitalier Departemental Vendee

Status

Completed

Conditions

Delivery

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT04897451
CHD21-0028

Details and patient eligibility

About

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.

Enrollment

160 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Woman who experienced at least one method of cervical ripening in our hospital

Exclusion criteria

  • Patient's refusal

Trial design

160 participants in 1 patient group

Women with cervical ripening in the context of artificial labor induction
Treatment:
Other: Questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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