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Intramuscular Oxytocics: A Randomised Control Trial (IMox)

Primary Purpose

Post Partum Haemorrhage

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
Carbetocin
Syntocinon
Syntometrine
Sponsored by
North Bristol NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Carbetocin

Syntocinon

Syntometrine

Arm Description

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

Outcomes

Primary Outcome Measures

Requirement for additional uterotonic drugs within 24 hours of birth
Proportion of patients requiring additional uterotonic drugs after administration of study drug

Secondary Outcome Measures

Estimated volume of blood loss at delivery
Estimated volume of blood loss at delivery
Transfusion of blood products (type and number of units given)
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
The requirement for the placenta to be removed in theatre
Requirement for surgical intervention to manage PPH
As a result of significant PPH a surgical intervention was required to manage the PPH
Maternal hypertension
Hypertension
Maternal hypotension
BP <90/60
Maternally-reported health-related quality of life
health-related quality of life reported by mother
Abdominal pain in the first two postnatal hours, recorded in Case Report Form (CRF) by midwife
Patient reported secondary outcome
Post-partum vomiting
Patient reported secondary outcome
Need for anti-emetic
Patient reported secondary outcome By definition, labour starts when the patient is at least 3-4cm dilated with regular, painful contractions.
Headache
Patient reported secondary outcome
Maternal experience of side effects
Captured using maternal side effects questionnaire

Full Information

First Posted
July 25, 2014
Last Updated
November 9, 2018
Sponsor
North Bristol NHS Trust
Collaborators
Ferring Pharmaceuticals, University of Bristol, University of the West of England, Royal United Hospital Bath NHS Trust, Gloucestershire Hospitals NHS Foundation Trust, University Hospitals Bristol and Weston NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT02216383
Brief Title
Intramuscular Oxytocics: A Randomised Control Trial
Acronym
IMox
Official Title
Intramuscular Oxytocics: A Randomised Control Trial of Intramuscular Carbetocin, Syntocinon and Syntometrine for the Third Stage of Labour Following Vaginal Birth
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
February 2015 (undefined)
Primary Completion Date
August 31, 2018 (Actual)
Study Completion Date
October 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
North Bristol NHS Trust
Collaborators
Ferring Pharmaceuticals, University of Bristol, University of the West of England, Royal United Hospital Bath NHS Trust, Gloucestershire Hospitals NHS Foundation Trust, University Hospitals Bristol and Weston NHS Foundation Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Partum Haemorrhage
Keywords
Post partum haemorrhage, Active Management of Third Stage of Labour, Carbetocin, Syntocinon, Syntometrine, Birth experience, Labour

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
5798 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Carbetocin
Arm Type
Experimental
Arm Description
One dose of 100 micrograms intramuscular Carbetocin given for active management of the third stage of labour, immediately after the birth of the baby
Arm Title
Syntocinon
Arm Type
Active Comparator
Arm Description
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
Arm Title
Syntometrine
Arm Type
Active Comparator
Arm Description
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
Intervention Type
Drug
Intervention Name(s)
Carbetocin
Other Intervention Name(s)
Pabal
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Syntocinon
Other Intervention Name(s)
Oxytocin
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Syntometrine
Other Intervention Name(s)
Syntometrine 500 micrograms/5 IU Solution for Injection
Intervention Description
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.
Primary Outcome Measure Information:
Title
Requirement for additional uterotonic drugs within 24 hours of birth
Description
Proportion of patients requiring additional uterotonic drugs after administration of study drug
Time Frame
From administration of prophylactic uterotonic agent to discharge from labour ward, within an expected average of 6 hours.
Secondary Outcome Measure Information:
Title
Estimated volume of blood loss at delivery
Description
Estimated volume of blood loss at delivery
Time Frame
Within 24 hours of delivery
Title
Transfusion of blood products (type and number of units given)
Description
Number of units of blood transfused, or volume of own blood returned to patient if intraoperative cell salvage used
Time Frame
From delivery until transfer from Labour Ward, within an expected average of 6 hours.
Title
Manual removal of placenta in theatre
Description
The requirement for the placenta to be removed in theatre
Time Frame
From delivery until transfer from Labour Ward
Title
Requirement for surgical intervention to manage PPH
Description
As a result of significant PPH a surgical intervention was required to manage the PPH
Time Frame
From delivery until transfer from Labour Ward, within an expected average of 2 days
Title
Maternal hypertension
Description
Hypertension
Time Frame
First two postnatal hours following administration of study drug
Title
Maternal hypotension
Description
BP <90/60
Time Frame
In first two postnatal hours
Title
Maternally-reported health-related quality of life
Description
health-related quality of life reported by mother
Time Frame
24 hours after delivery and 14 days after delivery
Title
Abdominal pain in the first two postnatal hours, recorded in Case Report Form (CRF) by midwife
Description
Patient reported secondary outcome
Time Frame
First 2 post natal hours
Title
Post-partum vomiting
Description
Patient reported secondary outcome
Time Frame
First 2 post natal hours
Title
Need for anti-emetic
Description
Patient reported secondary outcome By definition, labour starts when the patient is at least 3-4cm dilated with regular, painful contractions.
Time Frame
First 2 post natal hours
Title
Headache
Description
Patient reported secondary outcome
Time Frame
First two post natal hours
Title
Maternal experience of side effects
Description
Captured using maternal side effects questionnaire
Time Frame
In first two post natal hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tim Draycott, BMBS
Organizational Affiliation
North Bristol NHS Trust/University of Bristol
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Helen van der Nelson, BMBS
Organizational Affiliation
North Bristol NHS Trust/University of Bristol
Official's Role
Study Chair
Facility Information:
Facility Name
North Bristol NHS Trust
City
Bristol
State/Province
Avon
ZIP/Postal Code
BS10 5NB
Country
United Kingdom
Facility Name
Gloucestershire Hospitals NHS Trust
City
Gloucester
State/Province
Gloucestershire
ZIP/Postal Code
GL1 3NN
Country
United Kingdom
Facility Name
Royal United Hospital NHS Trust
City
Bath
State/Province
Somerset
ZIP/Postal Code
BA1 3NG
Country
United Kingdom
Facility Name
Nottingham University Hospitals NHS Trust
City
Nottingham
Country
United Kingdom
Facility Name
Great Western Hospital
City
Swindon
ZIP/Postal Code
SN3 6BB
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
30606246
Citation
van der Nelson H, O'Brien S, Lenguerrand E, Marques E, Alvarez M, Mayer M, Burnard S, Siassakos D, Draycott T. Intramuscular oxytocin versus oxytocin/ergometrine versus carbetocin for prevention of primary postpartum haemorrhage after vaginal birth: study protocol for a randomised controlled trial (the IMox study). Trials. 2019 Jan 3;20(1):4. doi: 10.1186/s13063-018-3109-2.
Results Reference
derived

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Intramuscular Oxytocics: A Randomised Control Trial

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