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Reducing primary and secondary cesarean delivery rates in women with a previous cesarean delivery using electrohysterography: randomized controlled trial

Reducing primary and secondary cesarean delivery rates in women with a previous cesarean delivery using electrohysterography: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26343
Enrollment
100
Registered
2019-12-02
Start date
2017-11-22
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trial of labor after previous cesarean delivery

Interventions

Electrohysterography as method of monitoring uterine activity during a trial of labor after previous cesarean delivery

Sponsors

Máxima MC Veldhoven
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Pregnant women aged 18 years or older with previous CD - Singleton pregnancy - 37 to 41 weeks of gestation - Cephalic presentation - Spontaneous onset of labor All patients included for this study must provide informed consent.

Exclusion criteria

Exclusion criteria: - Estimated fetal weight >4000g - Maternal age above 40 years - Classical vertical or T- or J-incision of uterus - Previous uterine rupture - Cesarean delivery in previous 12 months - Labor dystocia or failed induction as indication for previous cesarean delivery - Placenta praevia, vasa praevia, fetus with relevant congenital malformation that can influence the delivery mode - Primary infection of genital herpes simplex or active HIV - Suspicion for abruptio placentae - Dermatologic diseases, external or internal electrical stimulator and water birth.

Design outcomes

Primary

MeasureTime frame
Percentage of successful TOL will be the primary outcome measure in this study.

Secondary

MeasureTime frame
Secondary outcome measures will be reason for secondary CD, percentage instrumental vaginal deliveries, oxytocin augmentation, complications during delivery (e.g. uterine ruptures), maternal blood loss, duration of first and second phase of labor, neonatal outcomes such as Apgar score 12, admission to neonatal intensive care unit and perinatal mortality.

Contacts

Public ContactMarion Frenken

Máxima Medisch Centrum, Veldhoven

marion.frenken@mmc.nl040-8888380

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)