Implementation of AFL Monitoring in Clinical Use
Labour Dystocia
About this trial
This is an interventional supportive care trial for Labour Dystocia
Eligibility Criteria
Inclusion Criteria:
- gestational age at least 37 + 0 weeks
- singleton pregnancy
- cephalic presentation
- active labor (regular painful contractions, effaced cervix open at least 3cm)
- arrested labour progress according partogram and clinic guidelines
Exclusion Criteria:
- intra uterine fetal growth retardation (> 22%)
- intra uterine fetal death
- threat of fetal asphyxia
- severe vaginal bleeding
- disproportion between the fetal head and the mother's pelvis
- hypertonic contractions (more than 5 in 10 minutes)
- known allergy or hypersensitivity to oxytocin or to any of derivatives
- women who cannot understand the information of the study
Sites / Locations
Arms of the Study
Arm 1
Arm 2
No Intervention
Active Comparator
A, Non-bicarbonate
B, Bicarbonate group
When labour arrest is diagnosed and the first AFL > 12 mmol/L the participants will be randomized to two groups. In group A the labour is treated according to the hospital's current guidelines during labour arrest, i.e. the stimulation with oxytocin is started and AFL is measured again after one hour
When labour arrest is diagnosed and the first AFL > 12 mmol/L the participants will be randomized to two groups. In group B the participant will drink bicarbonate (2 packages of Samarin®) dissolved in 200 ml of water. Then after one hour the AFL will be measured again and the stimulation with oxytocin will be started if there is no progress in the cervix.