Induced; Birth

2

Review clinical trials related to Induced; Birth. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Papaverine and Oxytocin vs Oxytocin Alone in Labor Induction

This study aims to evaluate the efficacy and safety of combining papaverine with oxytocin for labor induction compared to oxytocin alone

Participants needed: 126
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Western Galilee Hospital-NahariyaUpdated: Sep 19, 2024
Eligibility criteria

Women with a singleton pregnancy Over the age of 18 Term (between 37-42 weeks of...

parity >1 [+1]

Status: Recruiting

SAINT: Safe Induction of Labor Trial

Over the past years, the rates of labor induction have increased steadily, and at present more than one in four births occurs after induced labor in Norway. There is evidence that several groups of women benefit from labor induction, including those with preeclampsia (1), postdate pregnancy, diabetes, a large-for-gestational-age fetus, gestational diabetes, prelabor rupture of membranes at term, preterm prelabor rupture of membranes, twin pregnancy and intrahepatic cholestasis of pregnancy. At the same time, induction of labor is an independent risk factor for adverse obstetric outcomes, including cesarean section, operative vaginal delivery, chorioamnionitis, labor dystocia, prolonged labor, uterine rupture, and neonatal pH \< 7.10. A recent Norwegian nationwide clinical practice pilot evaluation demonstrated that the rate of intervention was high, and that as many as 44% of women with labor induction experienced operative delivery. Given that induction of labor is a common procedure (15 000 women per year in Norway) and increases risk of several major obstetric complications, interventions that may reduce operative births and facilitate safe deliveries are highly warranted. Bicarbonate and butylscopolamine bromide have been used in smaller studies in order to shorten labor. The medications seem to be safe with a low frequency of adverse events. The rationale of the present study is therefore to assess the efficacy of oral bicarbonate and intravenous butylscopolamine bromide on facilitating spontaneous (non-operative) delivery in pregnant female participants with induction of labor.

Participants needed: 3,000
Trial details
Phase: Phase 3Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Oslo University HospitalUpdated: Apr 4, 2024Locations: 5
Eligibility criteria

Participant must be between 18 and 50 years of age at the time of signing the in... [+4]

Multiple gestation [+14]