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More info
You can access this
clinical trial
if you have
Birth; Delayed
and you are
between 18 and 60
years old
-
The phase for this study is not defined.
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The purpose

In a randomized control trial conducted in six study centers/labour wards in Sweden, consenting nulliparous women in active phase of labour and with a defined delayed labour progress will be randomized to receive a regimen of either high or low dose of oxytocin. Primary outcome is caesarean delivery rate. Secondary outcomes are: Apgar score, need of neonatal intensive care, hyper-stimulation of contractions, spontaneous vaginal birth rate, length of labour, postpartum haemorrhage, sphincter lacerations, experienced labour pain, epidural analgesia and the women´s childbirth experience one month postpartum (assessed with Childbirth Experience Questionnaire). Study results will contribute to establish good evidence-based routines regarding oxytocin treatment of delayed labour progress.

Provided treatments

  • Drug: Oxytocin

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01587625. The sponsor of the trial is Göteborg University and it is looking for 1376 volunteers for the current phase.
Official trial title:
High Dose Versus Low Dose Oxytocin for Augmentation of Delayed Labour