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Induction to Labour With Double Cervical Ballon at Home Versus at Hospital — INDOBAMHOS  

Induced; Birth Clinical Trial

Official title:
Induction to Labour With Double Cervical Ballon at Home Versus at Hospital to Improve the Vaginal Delivery Rate, Maternal Satisfaction and Reduce Costs: Multicentric Randomized Clinical Trial

Clinical Trial Summary

The goal of this clinical trial] is to compare the outcomes between induction to labour at home versus hospitalized. The main questions it aims to answer are: - Can the induction to labour at home with cervical rippening ballon increase the vaginal delivery rate? - Will the induction to labour at home increase maternal satisfaction - Will the induction to labour at home improve medical circuits and coulb it be cost effective? Participants who meet inclusion criteria will undergo randomization so as to be asignated an induction to labour at home or in the hospital. Researchers will compare both labour induction groups to see if the induction to labour at home has better outcomes as described previously.

Clinical Trial Description

INDOBAMHOS is a multicentric randomized clinical trial which is based in the principle that cervical rippening with intracervical probes with ballons is as safe as pharmacological induction with PGE2 and it seems to be a suitable option to develop the cervical rippening process of the induction at home rather than in the hospital. The purpouse of the study is to demonstrate that the comfort of performing the cervical rippenning at home will benefit patients with an increase of the vaginal delivery rate and increases maternal satisfaction. And also will improve medical circuits and could be cost-effective when compared to hospitalized labour induction. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06053073
Study type Interventional
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact Maria del Carmen Medina Mallén
Phone 0034646337446
Email mmedinam@santpau.cat
Status Recruiting
Phase N/A
Start date March 27, 2023
Completion date March 2026
View Details
See also
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