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Labour Induction clinical trials

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NCT ID: NCT04514770 Completed - Labour Induction Clinical Trials

Impact of Early Versus Late Amniotomy on Labour Induction in Nulliparous Women After Vaginal Misoprostol

RCT
Start date: May 3, 2019
Phase: N/A
Study type: Interventional

Investigation the effect of timing of amniotomy (early versus delayed) after vaginal misoprostol in induced labor. Condition: induction of labour intervention: eary versus late amniotomy on labour induction after vaginal misoprostol Phase: Not applicable

NCT ID: NCT03016208 Completed - Labour Induction Clinical Trials

The Misoprostol Vaginal Insert for Labour Induction

Start date: May 2015
Phase: N/A
Study type: Observational

Objective: To compare the efficacy and safety of the misoprostol vaginal insert (MVI) for labour induction using standard (MVI-24) and adjusted (MVI-10) criteria. Design: Non-interventional observational case control study. Setting: Tertiary-care academic centre in Germany. Population: A cohort of 138 pregnant women ≥ 37/0 weeks undergoing labour induction. Methods: Induction of labour with MVI in a consecutive series of women using standard (MVI-24, n = 69) or adjusted (MVI-10, n = 69) criteria. Main outcome measures: The primary outcomes were the time from induction to delivery and the caesarean section rate. The secondary outcomes included the need for additional measures to induce labour, uterine tachysystole, tocolysis, fetal scalp blood testing, meconium-stained amniotic fluid, umbilical arterial pH, and Apgar score.

NCT ID: NCT02904317 Completed - Labour Induction Clinical Trials

Misoprostol for Labour Induction

Start date: August 2015
Phase: N/A
Study type: Observational

Objective: To compare the efficacy and safety of the misoprostol vaginal insert (MVI) with an off-label use of oral misoprostol (OM). Design: Pair-matched case-control study. Setting: Tertiary-care academic centre in Germany. Population: A cohort of 138 women ≥ 37/0 weeks pregnant undergoing labour induction. Methods: The induction of labour with a retrievable prostaglandin vaginal insert in a consecutive series of 69 women was compared with induction using oral misoprostol in a pair-matched cohort. Main outcome measures: The primary outcomes were the time from induction to delivery and the caesarean section rate. Secondary outcomes included uterine tachysystole, tocolysis, fetal scalp blood testing, meconium-stained amniotic fluid, umbilical arterial pH, and Apgar score.

NCT ID: NCT02539199 Completed - Labour Induction Clinical Trials

Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour

Start date: September 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the effectiveness and safety of vaginally administered misoprostol (Misodel) versus per orally administered misoprostol (Cytotec) in induction of labour in nulliparous women.

NCT ID: NCT02168881 Recruiting - Labour Induction Clinical Trials

Oral Misoprostol Versus Vaginal Dinoprostone For Induction Of Labour: A Randomized Controlled Clinical Trial

Start date: May 2014
Phase: N/A
Study type: Interventional

This study is to compare between oral misoprostol in solution and vaginal dinoprostone in induction of labour in primiparous women with singleton pregnancy as regards efficiency and safety to both mother and fetus.