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Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress

Primary Purpose

Postpartum Hemorrhage

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Oxytocin
Ergot
Carboprost
Sponsored by
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postpartum Hemorrhage focused on measuring pregnancy, postpartum hemorrhage, Cesarean delivery, failure to progress in labor

Eligibility Criteria

14 Years - 55 Years (Child, Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • patients who give written informed consent
  • patients undergoing Cesarean section for failure to progress in labour, under regional anesthesia
  • patients should be in the first stage of labour and have received oxytocin for at least 4 hours

Exclusion Criteria:

  • patients who refuse to give written informed consent
  • patients who require general anesthesia
  • patients who claim allergy or hypersensitivity to oxytocin, ergot derivatives or prostaglandins
  • patients with cardiac diseases and hypertension or preeclampsia ( diastolic blood pressure > 90 mmHg, systolic blood pressure > 140 mmHg )
  • patients with asthma or any other respiratory disease
  • patients with conditions at risk of PPH such as placenta previa, multiple gestation, preeclampsia, macrosomia, polyhydramnios, uterine fibroids, previous history of uterine atony and postpartum bleeding, bleeding diathesis and known infection.

Sites / Locations

  • Mount Sinai Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Oxytocin only

Oxytocin + Ergot

Oxytocin + Carboprost

Arm Description

Oxytocin 5IU IV bolus, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours

Oxytocin 5IU IV bolus + Ergot 0.25mg IV, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours

Oxytocin 5IU IV bolus + Carboprost 0.25mg IM, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours

Outcomes

Primary Outcome Measures

Need for additional uterotonics intraoperatively
Need for additional uterotonics intraoperatively if requested by the surgeon, YES or NO

Secondary Outcome Measures

Effectiveness of uterine contraction
Adequate/inadequate uterine tone at 3,5 & 10 min
Need for blood transfusion
Any blood products administered
Vital signs
In the OR, heart rate, blood pressure, and oxygen saturation will be measured and looked at for abnormalities
Side effects
The presence of nausea, vomiting,other dysrhythmias, chest pain, headache, bronchospasm and any others will be recorded.
Estimated blood loss
calculated blood loss = EBV (Pre-op Htc-Post-op Htc) EBV (estimated blood volume, mL)=patient's weight in kg x 85
Need for additional uterotonics or interventions post-operatively
Need for additional uterotonics or interventions post-operatively up to 24 hours post-partum

Full Information

First Posted
May 31, 2013
Last Updated
September 22, 2020
Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01869556
Brief Title
Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress
Official Title
Comparison of Intravenous Ergonovine With Intramuscular Carboprost, Both in Combination With Oxytocin Infusion, During Cesarean Section for Failure to Progress in Labor: A Double-blinded Placebo-controlled Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
June 4, 2013 (Actual)
Primary Completion Date
July 8, 2019 (Actual)
Study Completion Date
September 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients having Cesarean section after they have been in labor for many hours bleed much more, in average twice as much, as compared with patients having an elective Cesarean section. The investigators believe a simple change in practice might contribute to reduce this bleeding. This study will involve the use of oxytocin (also known as syntocinon), ergonovine (also known as ergot) and carboprost (also known as hemabate). Oxytocin is routinely used to help contract the uterus and keep it contracted after the delivery of the baby and placenta, so as to reduce the amount of blood loss. Ergonovine is also given through the intravenous line, while carboprost is given as an injection in the muscle. Although they are not routinely given in every case, these are very frequently given as rescue medications to patients who fail to respond appropriately to oxytocin. This study is designed to determine if ergonovine or carboprost given in association with oxytocin, in a preventive way, after delivery of the baby and placenta, can reduce the amount of blood loss during Cesarean sections following a trial of labour.
Detailed Description
The objective of the investigators study is to compare the efficacy of intravenous ergonovine and intramuscular carboprost, when administered with oxytocin infusion, prophylactically to decrease blood loss at Cesarean section for labor arrest. Desensitization of the oxytocin receptors has been recently demonstrated in cultured human myometrial cells after continuous and prolonged exposure to oxytocin in-vitro. This could be also the reason for a greater risk of uterine atony and postpartum hemorrhage (PPH) seen in women requiring induction and augmentation of labor. Therefore, addition of a different uterotonic agent, involving a different mechanism of action, to oxytocin infusion is likely to be beneficial, especially in women undergoing CS following failure to progress in labor, who are at a greater risk for PPH.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Hemorrhage
Keywords
pregnancy, postpartum hemorrhage, Cesarean delivery, failure to progress in labor

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
105 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oxytocin only
Arm Type
Active Comparator
Arm Description
Oxytocin 5IU IV bolus, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours
Arm Title
Oxytocin + Ergot
Arm Type
Active Comparator
Arm Description
Oxytocin 5IU IV bolus + Ergot 0.25mg IV, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours
Arm Title
Oxytocin + Carboprost
Arm Type
Active Comparator
Arm Description
Oxytocin 5IU IV bolus + Carboprost 0.25mg IM, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours
Intervention Type
Drug
Intervention Name(s)
Oxytocin
Other Intervention Name(s)
syntocinon
Intervention Description
Oxytocin 5IU IV bolus, followed by an infusion of oxytocin 20IU/L, running at at rate of 40mIU/min for 8 hours
Intervention Type
Drug
Intervention Name(s)
Ergot
Other Intervention Name(s)
ergonovine maleate
Intervention Description
Ergot 0.25mg IV
Intervention Type
Drug
Intervention Name(s)
Carboprost
Other Intervention Name(s)
Hemabate®
Intervention Description
Carboprost 0.25mg IM
Primary Outcome Measure Information:
Title
Need for additional uterotonics intraoperatively
Description
Need for additional uterotonics intraoperatively if requested by the surgeon, YES or NO
Time Frame
1 hour
Secondary Outcome Measure Information:
Title
Effectiveness of uterine contraction
Description
Adequate/inadequate uterine tone at 3,5 & 10 min
Time Frame
10 min
Title
Need for blood transfusion
Description
Any blood products administered
Time Frame
24 hours
Title
Vital signs
Description
In the OR, heart rate, blood pressure, and oxygen saturation will be measured and looked at for abnormalities
Time Frame
2 hours
Title
Side effects
Description
The presence of nausea, vomiting,other dysrhythmias, chest pain, headache, bronchospasm and any others will be recorded.
Time Frame
24 hours
Title
Estimated blood loss
Description
calculated blood loss = EBV (Pre-op Htc-Post-op Htc) EBV (estimated blood volume, mL)=patient's weight in kg x 85
Time Frame
48 hours
Title
Need for additional uterotonics or interventions post-operatively
Description
Need for additional uterotonics or interventions post-operatively up to 24 hours post-partum
Time Frame
24 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: patients who give written informed consent patients undergoing Cesarean section for failure to progress in labour, under regional anesthesia patients should be in the first stage of labour and have received oxytocin for at least 4 hours Exclusion Criteria: patients who refuse to give written informed consent patients who require general anesthesia patients who claim allergy or hypersensitivity to oxytocin, ergot derivatives or prostaglandins patients with cardiac diseases and hypertension or preeclampsia ( diastolic blood pressure > 90 mmHg, systolic blood pressure > 140 mmHg ) patients with asthma or any other respiratory disease patients with conditions at risk of PPH such as placenta previa, multiple gestation, preeclampsia, macrosomia, polyhydramnios, uterine fibroids, previous history of uterine atony and postpartum bleeding, bleeding diathesis and known infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mrinalini Balki, MD
Organizational Affiliation
MOUNT SINAI HOSPITAL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G1X5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
33543897
Citation
Balki M, Downey K, Walker A, Seaward G, Carvalho JCA. Prophylactic Administration of Uterotonics to Prevent Postpartum Hemorrhage in Women Undergoing Cesarean Delivery for Arrest of Labor: A Randomized Controlled Trial. Obstet Gynecol. 2021 Mar 1;137(3):505-513. doi: 10.1097/AOG.0000000000004288.
Results Reference
derived

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Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress

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