Clinical Trials Directory

Trials / Completed

CompletedNCT04244747

Labor Induction After Cesarean Section: Outcome, Hormonal Trends

The Hormonal Milieu With Different Methods of Labour Induction: a Prospective Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Western Galilee Hospital-Nahariya · Other Government
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Objectives- To compare changes in labour-associated maternal and fetal hormone levels during breast stimulation, balloon induction and spontaneous labour. To compare efficacy and safety of labour induction methods in women with previous caesarean section. Design- Participants were randomized to undergo induction of labour by breast stimulation or intracervical balloon compared to spontaneous labour (controls). Setting- A single tertiary hospital Population- women at term, with previous caesarean section

Detailed description

Maternal serum levels of oxytocin, prostaglandin F2α, prostaglandin E2, prolactin, estradiol and cortisol levels were analyzed at 0, 3 and 6 hours post induction initiation, including the two groups catheter balloon and breast stimulation and controls in spontaneous labor. Fetal umbilical cord hormones were measured in the three mentioned above groups. Clinical outcomes were documented in the two induction groups.

Conditions

Interventions

TypeNameDescription
DEVICEinduction of labor by breast stimulation
DEVICEinduction of labor by catheter balloon

Timeline

Start date
2016-01-01
Primary completion
2018-07-01
Completion
2020-01-01
First posted
2020-01-28
Last updated
2021-04-13

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT04244747. Inclusion in this directory is not an endorsement.