Trials / Completed
CompletedNCT05096104
Patient Satisfaction During Artificial Induction of Labor by Cervical Ripening
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 800 (actual)
- Sponsor
- University Hospital, Strasbourg, France · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- —
Summary
20% of deliveries take place following an artificial induction of labor. The latter sometimes requires prior cervical ripening, of which the two most widely used methods in France are oral misoprostol and the balloon catheter, left to the discretion of clinicians. The objective of this study is to observe which cervical maturation method patients choose when an artificial induction of labor with an unfavorable cervical status must be carried out, and to observe the patient's criteria as to the choice made, as well as their experience and their satisfaction with artificial induction of labor, in order to improve our clinical practices, the experience of childbirth, and promote patient autonomy.
Conditions
Timeline
- Start date
- 2021-08-06
- Primary completion
- 2022-06-08
- Completion
- 2022-08-08
- First posted
- 2021-10-27
- Last updated
- 2023-12-12
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT05096104. Inclusion in this directory is not an endorsement.