Intramuscular Oxytocics: A Randomised Control Trial (IMox)
Post Partum Haemorrhage
About this trial
This is an interventional prevention trial for Post Partum Haemorrhage focused on measuring Post partum haemorrhage, Active Management of Third Stage of Labour, Carbetocin, Syntocinon, Syntometrine, Birth experience, Labour
Eligibility Criteria
Inclusion Criteria:
- ≥18 years of age at time of delivery
- Singleton pregnancy
- Vaginal birth (spontaneous and instrumental)
- >24 weeks gestation
Exclusion Criteria:
- Significant APH (>50ml) or suspected or proven placenta abruption
- Maternal coagulation disorder
- Intrauterine fetal death
- Patients who would decline blood products if required
- Known or suspected hypertensive disorders, including pre-eclampsia, pregnancy induced hypertension, essential hypertension (even if blood pressure well controlled)
- Hypertension in labour, or patients who have not had their blood pressure checked in labour
- Patients with peripheral, hepatic or cardiac disease
- Patients with an allergy or hypersensitivity to any of the active ingredients in Carbetocin, Syntometrine or Syntocinon
- Epilepsy
Sites / Locations
- North Bristol NHS Trust
- Gloucestershire Hospitals NHS Trust
- Royal United Hospital NHS Trust
- Nottingham University Hospitals NHS Trust
- Great Western Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Active Comparator
Carbetocin
Syntocinon
Syntometrine
One dose of 100 micrograms intramuscular Carbetocin given for active management of the third stage of labour, immediately after the birth of the baby
One dose of 10 International Units intramuscular Syntocinon given for active management of the third stage of labour, immediately after the birth of the baby
One dose of 500micrograms/5 International Units intramuscular Syntometrine given for active management of the third stage of labour, immediately after the birth of the baby