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Patient Satisfaction During Artificial Induction of Labor by Cervical Ripening

NCT05096104 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 800

Last updated 2023-12-12

No results posted yet for this study

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

  • Cervical Ripening

Sponsors & Collaborators

  • University Hospital, Strasbourg, France

    lead OTHER

Principal Investigators

  • Nicolas SANANES, MD, PhD · Service de gynécologie Obstétrique - Hôpitaux Universitaires de Strasbourg

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-06
Primary Completion
2022-06-08
Completion
2022-08-08

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05096104 on ClinicalTrials.gov