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| ID | Type | Description | Link |
|---|---|---|---|
| 2014-001948-37 | EudraCT Number |
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| Name | Class |
|---|---|
| Ferring Pharmaceuticals | INDUSTRY |
| University of Bristol | OTHER |
| University of the West of England | OTHER |
| Royal United Hospital Bath NHS Trust |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Carbetocin | Experimental | One dose of 100 micrograms intramuscular Carbetocin given for active management of the third stage of labour, immediately after the birth of the baby |
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| Syntocinon | Active Comparator | 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 |
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| Syntometrine | Active Comparator | 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 |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Carbetocin | Drug | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Requirement for additional uterotonic drugs within 24 hours of birth | Proportion of patients requiring additional uterotonic drugs after administration of study drug | From administration of prophylactic uterotonic agent to discharge from labour ward, within an expected average of 6 hours. |
| Measure | Description | Time Frame |
|---|---|---|
| Estimated volume of blood loss at delivery | Estimated volume of blood loss at delivery | Within 24 hours of 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Tim Draycott, BMBS | North Bristol NHS Trust/University of Bristol | Study Director |
| Helen van der Nelson, BMBS | North Bristol NHS Trust/University of Bristol | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| North Bristol NHS Trust | Bristol | Avon | BS10 5NB | United Kingdom | ||
| Gloucestershire Hospitals NHS Trust |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 30606246 | Derived | 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. |
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| ID | Term |
|---|---|
| D006473 | Postpartum Hemorrhage |
| ID | Term |
|---|---|
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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| ID | Term |
|---|---|
| C020731 | carbetocin |
| D010121 | Oxytocin |
| C038346 | syntometrine |
| D007267 | Injections |
| ID | Term |
|---|---|
| D010909 | Pituitary Hormones, Posterior |
| D010907 | Pituitary Hormones |
| D036361 | Peptide Hormones |
| D006728 | Hormones |
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| OTHER |
| Gloucestershire Hospitals NHS Foundation Trust | OTHER |
| University Hospitals Bristol and Weston NHS Foundation Trust | OTHER |
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|
| Syntocinon | Drug | 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. |
|
|
| Syntometrine | Drug | 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. |
|
|
| From delivery until transfer from Labour Ward, within an expected average of 6 hours. |
| Manual removal of placenta in theatre | The requirement for the placenta to be removed in theatre | From delivery until transfer from Labour Ward |
| Requirement for surgical intervention to manage PPH | As a result of significant PPH a surgical intervention was required to manage the PPH | From delivery until transfer from Labour Ward, within an expected average of 2 days |
| Maternal hypertension | Hypertension | First two postnatal hours following administration of study drug |
| Maternal hypotension | BP <90/60 | In first two postnatal hours |
| Maternally-reported health-related quality of life | health-related quality of life reported by mother | 24 hours after delivery and 14 days after delivery |
| Abdominal pain in the first two postnatal hours, recorded in Case Report Form (CRF) by midwife | Patient reported secondary outcome | First 2 post natal hours |
| Post-partum vomiting | Patient reported secondary outcome | First 2 post natal hours |
| 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. | First 2 post natal hours |
| Headache | Patient reported secondary outcome | First two post natal hours |
| Maternal experience of side effects | Captured using maternal side effects questionnaire | In first two post natal hours |
| Gloucester |
| Gloucestershire |
| GL1 3NN |
| United Kingdom |
| Royal United Hospital NHS Trust | Bath | Somerset | BA1 3NG | United Kingdom |
| Nottingham University Hospitals NHS Trust | Nottingham | United Kingdom |
| Great Western Hospital | Swindon | SN3 6BB | United Kingdom |
| D011644 | Puerperal Disorders |
| D014592 | Uterine Hemorrhage |
| D006470 | Hemorrhage |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006730 |
| Hormones, Hormone Substitutes, and Hormone Antagonists |
| D010455 | Peptides |
| D000602 | Amino Acids, Peptides, and Proteins |
| D004333 | Drug Administration Routes |
| D004358 | Drug Therapy |
| D013812 | Therapeutics |