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Prophylactic Methylergonovine for Twin Cesarean

Prophylactic Methylergonovine in Patients Undergoing Cesarean Delivery With Twin Gestations: A Randomized Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05772156
Enrollment
66
Registered
2023-03-16
Start date
2023-03-07
Completion date
2024-03-11
Last updated
2025-06-13

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

Conditions

Postpartum Hemorrhage, Twin; Complicating Pregnancy

Brief summary

Obstetrical hemorrhage (excessive bleeding related to pregnancy) is a leading cause of maternal morbidity (disease or symptom of disease) and mortality (death) worldwide with a significantly higher frequency and severity following cesarean delivery. Twin gestations (twin pregnancy) are at particularly higher risk for postpartum hemorrhage, yet the management of obstetrical bleeding following twin delivery remains identical to singleton delivery. The purpose of this study is to understand the effect of prophylactic methylergonovine on blood loss in scheduled twin pregnancy cesarean deliveries. Participants will be randomized (like tossing a coin) to Methylergonovine (investigational drug) or water with salt (saline) (placebo). Methylergonovine or saline will be given as an injection immediately after delivery.

Detailed description

Obstetrical hemorrhage is a leading cause of maternal morbidity and mortality worldwide with a significantly higher frequency and severity following cesarean delivery. In 2020, 31.9 percent of pregnant women in the United States underwent cesarean delivery, making it the second most common operation performed. Though multiple complications can occur following cesarean delivery, hemorrhage morbidities are among the most common with significant cardiovascular implications. Twin gestations are at particularly higher risk for postpartum hemorrhage due to impaired myometrial contractility and atony following overdistention; increased maternal blood volume; and increased uterine blood flow compared to singletons, yet the management of obstetrical bleeding following twin delivery remains identical to singleton delivery. Current strategies to address intrapartum hemorrhage have relied on pharmacological and mechanical treatments after intraoperative identification. However, there is extensive work on prophylactic therapies administered intraoperatively to prevent obstetrical hemorrhage. Recent evidence has emerged about the utility of prophylactic Methylergonovine for the prevention of obstetrical hemorrhage. Methylergonovine, a semisynthetic ergot alkaloid, acts primarily on alpha adrenergic receptors of uterine and vascular smooth muscle, increasing uterine tone and promoting vasoconstriction. In a randomized trial of 80 women undergoing intrapartum cesarean delivery found that fewer patients who were allocated to the methylergonovine group received additional uterotonic agents (20% vs 55%, relative risk (RR) 0.4, 95% confidence interval (CI) 0.2-0.6). Participants receiving methylergonovine were more likely to have satisfactory uterine tone (80% vs 41%, RR 1.9, 95% CI 1.5-2.6), lower incidence of postpartum hemorrhage (35% vs 59%, RR 0.6, 95% CI 0.4-0.9), lower mean quantitative blood loss (967 mL vs 1,315 mL; mean difference 348, 95% CI 124-572), and a lower frequency of blood transfusion (5% vs 23%, RR 0.2, 95% CI 0.1-0.6). Investigators concluded that the administration of prophylactic methylergonovine in addition to oxytocin in patients undergoing intrapartum cesarean birth reduces the need for additional uterotonic agents. In a prospective study of 1210 participants found that intraoperative, prophylactic methylergonovine decreased post-operative blood loss with no adverse side effects. Randomized trials of Methylergonovine as prophylaxis to prevent hemorrhage in cesarean delivery have exclude twin gestations. Currently, there remains a paucity of research regarding prophylactic procedures for twin cesarean delivery. There is an opportunity to prophylactically address hemorrhage in high-risk groups. Therefore, the investigators propose a prospective randomized controlled trial which will compare maternal blood loss associated with prophylactic methylergonovine during cesarean delivery among patients with twin.

Interventions

Methylergonovine 200mcg Intramuscular (IM)

DRUGPlacebo

Matching saline placebo

Sponsors

Columbia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
FEMALE
Age
No minimum to 65 Years
Healthy volunteers
No

Inclusion criteria

* Twin gestation * Scheduled cesarean delivery (\>=34 weeks)

Exclusion criteria

* Patients with known hypertensive disease: history of chronic hypertension, gestational hypertension or preeclampsia with or without severe features * Use of protease inhibitors given known vasoconstrictive side effects with concomitant methylergonovine administration * Hypersensitivity to methylergonovine or any of the ingredients * Participating in another intervention study where the primary outcome includes postpartum bleeding or thromboembolism, or the study intervention directly affects postpartum bleeding or thromboembolism * Receipt of uterotonics, other than oxytocin, or planned or expected use of uterotonic prophylaxis * Non-elective cesarean delivery

Design outcomes

Primary

MeasureTime frameDescription
Change in Maternal Hemoglobin LevelBaseline and Postoperative Day 1 (Approximately 48 hours)The change in maternal hemoglobin level as taken from blood samples. The change will be calculated from preoperative day 1 (baseline) to postoperative day 1.

Secondary

MeasureTime frameDescription
Estimated Blood LossIntraoperative (Approximately 24 hours)At the end of the surgery, the primary surgeon will estimate the blood loss throughout the case.
Quantitative Blood LossIntraoperative (Approximately 24 hours)Quantitative blood loss is calculated by weighing the used towels during the operation. The number is calculated by the circulating nurse in the operating room.
Number of Participants With Postpartum HemorrhageIntraoperative (Approximately 24 hours)The number of participants with postpartum hemorrhage (defined as estimated blood loss \>1000 cc)
Number of Participants Requiring Use of UterotonicsIntraoperative (Approximately 24 hours)Number of participants given uterotonics, such as prostaglandins
Number of Participants Requiring Use of Tranexamic AcidIntraoperative (Approximately 24 hours)Number of participants given Tranexamic acid
Number of Participants Requiring Use of Open-Label MethylergonovineIntraoperative (Approximately 24 hours)Number of participants requiring the use of any amount of open-label methylergonovine (not blinded study drug)
Number of Participants Requiring Transfusion (Intraoperative)Intraoperative (Approximately 24 hours)Number of participants requiring transfusion of 1 or more units of packed red blood cells, including whole blood or cell saver.
Number of Participants With Surgical or Radiological InterventionsIntraoperative (Approximately 24 hours)Composite number of surgical or radiological interventions (such as: laparotomy, evacuation of hematoma, hysterectomy, uterine packing, intrauterine balloon tamponade, interventional radiology) to control bleeding and related complications or maternal death.
Surgical TimeIntraoperative (Approximately 24 hours)Surgical time measured from the time of incision to closure
Number of Participants Requiring Transfusion (6 Weeks)6 weeksNumber of participants requiring transfusion of 1 or more units of fresh frozen plasma, cryoprecipitate, or platelets or administration of any factor concentrates.
Number of Participants With Acute Elevation of Serum Creatinine48 hoursNumber of participants with acute elevation of serum creatinine of ≥ 0.3 mg/dL
Number of Postpartum Infectious Complications6 weeksNumber of Postpartum infectious complications such as: endometritis, surgical site infection, pelvic abscess
Number of Participants With Admission to the Intensive Care Unit6 weeksNumber of participants with admission to the intensive care unit for more than 24 hours
Length of StayUp to 6 weeksLength of stay measured from the time of hospital admission to hospital discharge.
Number of Participants Re-Admitted to the Hospital6 weeksThe number of participants who experienced hospital re-admission
Apgar Scores1 and 5 minutes post-delivery (approximately 24 hours post-baseline)Apgar score is a measure of the physical condition of a newborn infant. Scores range from 0-10 with a higher score indicating a better outcome; Apgar score of 0-3 is low, 4-6 is moderately abnormal, and 7-10 is reassuring.
Neonatal Intensive Care Unit (NICU) AdmissionTime of delivery (Approximately 24 hours)Number of newborns admitted to the neonatal intensive care unit (NICU).
Number of Participants With Transfusion Related Acute Lung Injury (TRALI)6 weeksNumber of participants with transfusion related acute lung injury (TRALI)

Countries

United States

Participant flow

Participants by arm

ArmCount
Prophylactic Methylergonovine
Prophylactic methylergonovine 200mcg IM
33
Placebo
Normal Saline 1mL
33
Total66

Baseline characteristics

CharacteristicProphylactic MethylergonovinePlaceboTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
33 Participants33 Participants66 Participants
Chorionicity, n (%)
Dichorionic
21 Participants21 Participants42 Participants
Chorionicity, n (%)
Monochorionic-Diamniotic
12 Participants12 Participants24 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
15 Participants14 Participants29 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
18 Participants19 Participants37 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Gestational diabetes mellitus, n (%)5 Participants6 Participants11 Participants
Maternal BMI (kg/m2), mean, SD30.0 kg/m^2
STANDARD_DEVIATION 5.7
30.5 kg/m^2
STANDARD_DEVIATION 7.3
30.25 kg/m^2
STANDARD_DEVIATION 6.5
Number of Prior Cesarean Deliveries, n (%)
0
23 Participants24 Participants47 Participants
Number of Prior Cesarean Deliveries, n (%)
1
7 Participants7 Participants14 Participants
Number of Prior Cesarean Deliveries, n (%)
>=2
3 Participants2 Participants5 Participants
Preoperative maternal hemoglobin level (g/dL), mean (SD)11.6 g/dL
STANDARD_DEVIATION 1.2
12.0 g/dL
STANDARD_DEVIATION 1.3
11.8 g/dL
STANDARD_DEVIATION 1.25
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants2 Participants2 Participants
Race (NIH/OMB)
Black or African American
11 Participants9 Participants20 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
22 Participants22 Participants44 Participants
Sex: Female, Male
Female
33 Participants33 Participants66 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants
Tobacco use in pregnancy, n (%)1 Participants0 Participants1 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 330 / 33
other
Total, other adverse events
0 / 330 / 33
serious
Total, serious adverse events
0 / 330 / 33

Outcome results

Primary

Change in Maternal Hemoglobin Level

The change in maternal hemoglobin level as taken from blood samples. The change will be calculated from preoperative day 1 (baseline) to postoperative day 1.

Time frame: Baseline and Postoperative Day 1 (Approximately 48 hours)

ArmMeasureValue (MEAN)Dispersion
Prophylactic MethylergonovineChange in Maternal Hemoglobin Level1.1 g/dLStandard Deviation 0.7
Placebo GroupChange in Maternal Hemoglobin Level2.1 g/dLStandard Deviation 0.9
Secondary

Apgar Scores

Apgar score is a measure of the physical condition of a newborn infant. Scores range from 0-10 with a higher score indicating a better outcome; Apgar score of 0-3 is low, 4-6 is moderately abnormal, and 7-10 is reassuring.

Time frame: 1 and 5 minutes post-delivery (approximately 24 hours post-baseline)

Population: Newborns were assessed rather than the mothers (i.e. enrolled participants). Each participant gave birth to twins (66 newborns total). Newborns were not considered enrolled but did contribute to this assessment.

ArmMeasureGroupValue (MEAN)
Prophylactic MethylergonovineApgar ScoresApgar 1 minute8 score on a scale
Prophylactic MethylergonovineApgar ScoresApgar 5 minutes9 score on a scale
Placebo GroupApgar ScoresApgar 1 minute8 score on a scale
Placebo GroupApgar ScoresApgar 5 minutes9 score on a scale
Secondary

Estimated Blood Loss

At the end of the surgery, the primary surgeon will estimate the blood loss throughout the case.

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (MEDIAN)
Prophylactic MethylergonovineEstimated Blood Loss800 cc
Placebo GroupEstimated Blood Loss1000 cc
Secondary

Length of Stay

Length of stay measured from the time of hospital admission to hospital discharge.

Time frame: Up to 6 weeks

ArmMeasureValue (MEDIAN)
Prophylactic MethylergonovineLength of Stay4 days
Placebo GroupLength of Stay4 days
Secondary

Neonatal Intensive Care Unit (NICU) Admission

Number of newborns admitted to the neonatal intensive care unit (NICU).

Time frame: Time of delivery (Approximately 24 hours)

Population: Newborns were assessed rather than the mothers (i.e. enrolled participants). Each participant gave birth to twins (66 newborns total). Newborns were not considered enrolled but did contribute to this assessment.

ArmMeasureValue (NUMBER)
Prophylactic MethylergonovineNeonatal Intensive Care Unit (NICU) Admission19 newborns
Placebo GroupNeonatal Intensive Care Unit (NICU) Admission20 newborns
Secondary

Number of Participants Re-Admitted to the Hospital

The number of participants who experienced hospital re-admission

Time frame: 6 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants Re-Admitted to the Hospital1 Participants
Placebo GroupNumber of Participants Re-Admitted to the Hospital3 Participants
Secondary

Number of Participants Requiring Transfusion (6 Weeks)

Number of participants requiring transfusion of 1 or more units of fresh frozen plasma, cryoprecipitate, or platelets or administration of any factor concentrates.

Time frame: 6 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants Requiring Transfusion (6 Weeks)2 Participants
Placebo GroupNumber of Participants Requiring Transfusion (6 Weeks)4 Participants
Secondary

Number of Participants Requiring Transfusion (Intraoperative)

Number of participants requiring transfusion of 1 or more units of packed red blood cells, including whole blood or cell saver.

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants Requiring Transfusion (Intraoperative)0 Participants
Placebo GroupNumber of Participants Requiring Transfusion (Intraoperative)0 Participants
Secondary

Number of Participants Requiring Use of Open-Label Methylergonovine

Number of participants requiring the use of any amount of open-label methylergonovine (not blinded study drug)

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants Requiring Use of Open-Label Methylergonovine0 Participants
Placebo GroupNumber of Participants Requiring Use of Open-Label Methylergonovine7 Participants
Secondary

Number of Participants Requiring Use of Tranexamic Acid

Number of participants given Tranexamic acid

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants Requiring Use of Tranexamic Acid2 Participants
Placebo GroupNumber of Participants Requiring Use of Tranexamic Acid7 Participants
Secondary

Number of Participants Requiring Use of Uterotonics

Number of participants given uterotonics, such as prostaglandins

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants Requiring Use of Uterotonics0 Participants
Placebo GroupNumber of Participants Requiring Use of Uterotonics6 Participants
Secondary

Number of Participants With Acute Elevation of Serum Creatinine

Number of participants with acute elevation of serum creatinine of ≥ 0.3 mg/dL

Time frame: 48 hours

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants With Acute Elevation of Serum Creatinine0 Participants
Placebo GroupNumber of Participants With Acute Elevation of Serum Creatinine0 Participants
Secondary

Number of Participants With Admission to the Intensive Care Unit

Number of participants with admission to the intensive care unit for more than 24 hours

Time frame: 6 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants With Admission to the Intensive Care Unit0 Participants
Placebo GroupNumber of Participants With Admission to the Intensive Care Unit0 Participants
Secondary

Number of Participants With Postpartum Hemorrhage

The number of participants with postpartum hemorrhage (defined as estimated blood loss \>1000 cc)

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants With Postpartum Hemorrhage6 Participants
Placebo GroupNumber of Participants With Postpartum Hemorrhage18 Participants
Secondary

Number of Participants With Surgical or Radiological Interventions

Composite number of surgical or radiological interventions (such as: laparotomy, evacuation of hematoma, hysterectomy, uterine packing, intrauterine balloon tamponade, interventional radiology) to control bleeding and related complications or maternal death.

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants With Surgical or Radiological Interventions0 Participants
Placebo GroupNumber of Participants With Surgical or Radiological Interventions0 Participants
Secondary

Number of Participants With Transfusion Related Acute Lung Injury (TRALI)

Number of participants with transfusion related acute lung injury (TRALI)

Time frame: 6 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Participants With Transfusion Related Acute Lung Injury (TRALI)0 Participants
Placebo GroupNumber of Participants With Transfusion Related Acute Lung Injury (TRALI)0 Participants
Secondary

Number of Postpartum Infectious Complications

Number of Postpartum infectious complications such as: endometritis, surgical site infection, pelvic abscess

Time frame: 6 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Prophylactic MethylergonovineNumber of Postpartum Infectious Complications0 Participants
Placebo GroupNumber of Postpartum Infectious Complications2 Participants
Secondary

Quantitative Blood Loss

Quantitative blood loss is calculated by weighing the used towels during the operation. The number is calculated by the circulating nurse in the operating room.

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (MEDIAN)
Prophylactic MethylergonovineQuantitative Blood Loss891 cc
Placebo GroupQuantitative Blood Loss1017 cc
Secondary

Surgical Time

Surgical time measured from the time of incision to closure

Time frame: Intraoperative (Approximately 24 hours)

ArmMeasureValue (MEDIAN)
Prophylactic MethylergonovineSurgical Time62.0 Minutes
Placebo GroupSurgical Time61.0 Minutes

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026