Current partner codePEPTIDESDE
NCT02216383·Phase 3·INTERVENTIONAL

Intramuscular Oxytocics: A Randomised Control Trial

Status

Completed

Phase

Phase 3

Enrollment

5,798

Locations

5

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

A quarter of all pregnancy and child-birth related deaths are due to excessive bleeding after the birth, "post-partum haemorrhage" (PPH). In the UK, PPH affects approx 10% of new mothers. PPH can be frightening for women and cause them to need additional treatments prolonging their hospital stay. Commonly PPH is caused by an inadequately contracted womb after childbirth. Giving the mother an injection of "uterotonic" medicine following the birth of their baby can prevent this. It reduces the risk of PPH by 66%. In the UK, the two medicines most commonly used are Syntocinon and Syntometrine. Syntometrine is longer acting, but a published review of trials concluded that Syntometrine is no better at preventing severe blood loss. Syntometrine is associated with more side effects including nausea, vomiting, and high blood pressure, and has been linked with rare, but fatal, cases of stroke. All guidelines therefore recommend Syntocinon for preventing PPH.Following a telephone survey of all maternity units in the UK, 71.4% of units still routinely use Syntometrine. Carbetocin is a newer medicine, already widely used after caesarean section, but not yet after vaginal birth. Other studies have shown that Carbetocin is slightly better at preventing bleeding after birth when compared to Syntometrine, has fewer side effects than Syntometrine, and that it may be just as good as Syntocinon at preventing PPH. No studies have directly compared all three medicines or compared their overall cost; information vital to the NHS. Investigators propose a trial of 5712 women over 13 months, in four maternity units to compare the effectiveness, side effects and cost of Syntocinon, Syntometrine and Carbetocin, for women having a vaginal birth. Women will be randomly allocated to receive one of these drugs. Women and staff will not know which drug they receive. Staff will collect data such as the number of extra drugs and treatments needed and the volume of blood lost. Women will be asked to complete a side effects questionnaire. Investigators will perform an analysis of cost effectiveness once all results are available. Aim: To directly compare the effectiveness, side effects and cost of Syntocinon, Syntometrine and Carbetocin given intramuscularly to prevent PPH in the 3rd stage of labour.

Full detailed description

BACKGROUND Around a quarter of all global pregnancy and child-birth related deaths are due to excessive bleeding after the birth of the baby and placenta, or "post-partum haemorrhage" (PPH). In the UK, PPH affects approximately 10% of new mothers. PPH can be extremely frightening for women and can cause them to need additional treatments including blood transfusion and removal of the womb as well as prolonging their hospital stay. The most common cause of PPH is an inadequately contracted womb after childbirth. Giving the mother an injection of "uterotonic" medicine following the birth of their baby can prevent this. It reduces the risk of PPH by 66% and this should routinely be offered to all labouring women. In the UK, the two medicines most commonly used for this purpose are Syntocinon and Syntometrine. Both mimic natural hormones. Syntometrine is longer acting, but a published review of trials comparing these two medicines concluded that Syntometrine is no better at preventing severe blood loss. Syntometrine is associated with more side effects including nausea, vomiting, and high blood pressure, and has been linked with rare, but fatal, cases of stroke. All guidelines therefore recommend Syntocinon for preventing PPH. Our group conducted a telephone survey of all maternity units in the UK, and found that 71.4% of units still routinely use Syntometrine. Investigators estimate that 40,000-70,000 women per year are experiencing distressing nausea and vomiting in the emotionally important first few hours following childbirth. These women are also receiving a medicine with the potential to cause dangerous high blood pressure. Carbetocin is a newer medicine, already widely used after caesarean section, but not yet after vaginal birth. Other studies have shown that Carbetocin is slightly better at preventing bleeding after birth when compared to Syntometrine, that it has fewer side effects than Syntometrine, and that it may be just as good as Syntocinon at preventing PPH. No studies have directly compared all three medicines or compared their overall cost; information vital to the NHS. METHOD Investigators propose a trial of 5712 women over 13 months, in four maternity units in the South-West to compare the effectiveness, side effects and cost of Syntocinon, Syntometrine and Carbetocin, for women having a vaginal birth. Women will be randomly allocated to receive one of these drugs. Women and staff will not know which drug they receive, so as not to influence the results collected. Staff will collect data such as the number of extra drugs and treatments needed and the volume of blood lost. Women will be asked to complete a side effects questionnaire. Investigators will perform an analysis of cost effectiveness once all results are available. AIMS To directly compare the effectiveness, side effects and cost of Syntocinon, Syntometrine and Carbetocin given intramuscularly to prevent PPH in the 3rd stage of labour.

Interventions

Treatment arms and agents.

DRUG

Carbetocin

The intervention is the administration of one dose of study drug to the recruited patient at the time of delivery. Carbetocin, listed here, is one of the of the three study drugs.

DRUG

Syntocinon

The intervention is the administration of one dose of study drug to the recruited patient at the time of delivery. Syntocinon, listed here, is one of the of the three study drugs.

DRUG

Syntometrine

The intervention is the administration of one dose of study drug to the recruited patient at the time of delivery. Syntometrine, listed here, is one of the of the three study drugs.

Timeline

From registration to results.

  1. First posted

    Aug 15, 2014

  2. Study start

    Feb 2015

  3. Primary completion

    Aug 31, 2018

  4. Study completion

    Oct 30, 2018

  5. Results posted

    Not reported

  6. Registry updated

    Nov 14, 2018

Outcomes

What the study measures.

Primary outcomes

Requirement for additional uterotonic drugs within 24 hours of birth

Time frame · From administration of prophylactic uterotonic agent to discharge from labour ward, within an expected average of 6 hours.

Proportion of patients requiring additional uterotonic drugs after administration of study drug

Secondary outcomes

Estimated volume of blood loss at delivery

Time frame · Within 24 hours of delivery

Estimated volume of blood loss at delivery

Transfusion of blood products (type and number of units given)

Time frame · From delivery until transfer from Labour Ward, within an expected average of 6 hours.

Number of units of blood transfused, or volume of own blood returned to patient if intraoperative cell salvage used

Manual removal of placenta in theatre

Time frame · From delivery until transfer from Labour Ward

The requirement for the placenta to be removed in theatre

Requirement for surgical intervention to manage PPH

Time frame · From delivery until transfer from Labour Ward, within an expected average of 2 days

As a result of significant PPH a surgical intervention was required to manage the PPH

Maternal hypertension

Time frame · First two postnatal hours following administration of study drug

Hypertension

Maternal hypotension

Time frame · In first two postnatal hours

BP \<90/60

Maternally-reported health-related quality of life

Time frame · 24 hours after delivery and 14 days after delivery

health-related quality of life reported by mother

Abdominal pain in the first two postnatal hours, recorded in Case Report Form (CRF) by midwife

Time frame · First 2 post natal hours

Patient reported secondary outcome

Post-partum vomiting

Time frame · First 2 post natal hours

Patient reported secondary outcome

Need for anti-emetic

Time frame · First 2 post natal hours

Patient reported secondary outcome By definition, labour starts when the patient is at least 3-4cm dilated with regular, painful contractions.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
FEMALE
Healthy volunteers
Yes

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

Study locations

5 registered sites.

United Kingdom. Showing up to 24 locations stored in the fast local snapshot.

North Bristol NHS Trust

Bristol, Avon, United Kingdom

Gloucestershire Hospitals NHS Trust

Gloucester, Gloucestershire, United Kingdom

Royal United Hospital NHS Trust

Bath, Somerset, United Kingdom

Nottingham University Hospitals NHS Trust

Nottingham, United Kingdom

Great Western Hospital

Swindon, United Kingdom

Related trials

More studies on Carbetocin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.