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RecruitingNCT05719467

SAINT: Safe Induction of Labor Trial

A Double-blind Randomized Placebo-controlled Four-arm Trial to Assess the Efficacy of Oral Bicarbonate and Intravenous Butylscopolamine Bromide to Facilitate Spontaneous (Non-operative) Delivery in Pregnant Female Participants With Induction of Labor

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
3,000 (estimated)
Sponsor
Oslo University Hospital · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGBuscopan 20 MG/ML Injectable Solution1 mL intravenously
DRUGSodium bicarbonate4 g orally
DRUGPlacebo4g orally
DRUGNacl 0.9%1 mL intravenously

Timeline

Start date
2023-01-03
Primary completion
2025-01-31
Completion
2027-12-31
First posted
2023-02-09
Last updated
2024-04-04

Locations

5 sites across 1 country: Norway

Source: ClinicalTrials.gov record NCT05719467. Inclusion in this directory is not an endorsement.