Skip to content

Carbetocin RTS for preventing postpartum haemorrhage: a randomized non-inferiority controlled trial.

A phase III, randomized, double-blind, active, controlled, multinational, multicentre, non-inferiority trial using carbetocin room temperature stable (RTS) for the prevention of postpartum haemorrhage during the third stage of labour in women delivering vaginally.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000870651
Acronym
CHAMPION
Enrollment
29645
Registered
2014-08-14
Start date
2015-07-07
Completion date
2018-01-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Postpartum haemorrhage (PPH) is the leading cause of maternal mortality in low-income countries and it contributes to nearly a quarter of maternal deaths globally. The majority of deaths due to PPH could be avoided through the use of prophylactic uterotonics during the third stage of labour and by timely and appropriate management. Oxytocin (IM/IV, 10 IU) is recommended as the uterotonic drug of choice. Based on the manufacturer’s recommendations, oxytocin should be stored under refrigeration. Carbetocin appears to be a promising agent in the prevention of PPH, is a more stable molecule and induces a prolonged uterine response, when administered postpartum. The manufacturer of carbetocin (Ferring Pharmaceuticals) has recently developed a room temperature stable formulation (carbetocin RTS) which makes it an attractive option for countries where maintaining the cold chain is problematic. The World Health Organization would like to evaluate the room temperature stable carbetocin solution for injection as a promising intervention for reducing PPH particularly in settings where cold storage is difficult to achieve and maintain.

Interventions

Carbetocin RTS 100 micrograms solution for intramuscular (IM) injection to be administered once during the third stage of labour.

Sponsors

World Health Organization
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
Yes

Inclusion criteria

*Women who are expected to deliver vaginally. *They have a cervical dilatation equal to or less than 6cm. *They provide written informed consent before any trial-related activities are carried out. *Known singleton pregnancy.

Exclusion criteria

Women will be excluded from participating in the trial if they are/have: *In an advanced first stage of labour (>6 cm cervical dilatation) or too distressed to understand, confirm and give informed consent regardless of cervical dilatation. *Non-emancipated minors (as per local regulations) without a guardian. *Scheduled for a planned caesarean section. *Birth considered an abortion according to local guidelines. *Allergic to carbetocin, other oxytocin homologues or excipients. *Serious cardiovascular disorders. *Not capable of giving consent due to other health problems such as obstetric emergencies (e.g. antepartum haemorrhage) or mental disorder. * Serious hepatic or renal disease * Epilepsy

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 13, 2026