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Study to Evaluate is ECV Success is Improved and the Side Effects Reduced With the Use of IV NTGL Versus Terbutaline

Intravenous Terbutaline Versus Intravenous Nitroglycerine for External Cephalic Version: A Double-Blinded Randomized Controlled Trial in Nulliparous Women

Status
Terminated
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02115256
Enrollment
6
Registered
2014-04-16
Start date
2014-07-31
Completion date
2015-04-30
Last updated
2017-06-14

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

Conditions

External Cephalic Version

Keywords

External Cephalic Version, breech

Brief summary

Breech presentation of a term pregnancy is a common occurrence. A procedure known as external cephalic version (ECV) is frequently used by obstetricians to turn the baby into the vertex position prior to delivery in order to avoid a cesarean section and the associated risks. Medications to relax the uterus, known as tocolytics, are used in conjunction with the procedure as they have been shown to improve the success rate of ECV, but with inconsistent, varying results.

Detailed description

Breech presentation occurs in approximately 3-4% of all births and all women with breech presentation at term undergo cesarean delivery. The only way to avoid a cesarean is to manually turn the baby prior to the date of delivery, a procedure known as elective external cephalic version (ECV). ECV has been shown to reduce the frequency of breech presentation at term and thus lessen the risks associated with breech delivery and those of cesarean section, with little risk to the mother or baby. Tocolysis, administered immediately prior to the ECV and commonly used at The Mount Sinai Hospital, has been shown to improve the success rate of ECV. Several different agents are known to cause tocolysis. These include beta-mimetics (ritodrine, terbutaline), nitroglycerine (NTGL) and nifedipine.Terbutaline has been shown to improve success rate of ECV. Another study published in 2004 by El-Sayed et al showed that subcutaneous terbutaline was associated with higher rates of successful ECV than IV NTGL in term patients. There is inconsistent data in regard to the success rate of ECV with NTGL. In a study published in 2003 by Bujold et al, NTGL was associated with a higher rate of side effects and a lower rate of successful ECV when compared to ritodrine. Another study published in 2009 by Hilton et al showed that NTGL was more efficacious for ECV in nulliparous versus multiparous women. Yet another study published in 2009 by Yanny et al showed no differences between sublingual NTGL versus placebo in efficacy, and reported no significant side effects. A study published in 2003 by Bujold et al showed that sublingual NTGL was associated with a higher incidence of headache and did not improve the success rate of ECV. It may be beneficial to use NTGL instead of terbutaline because NTGL is a shorter acting agent and the procedure itself only lasts 10-15 minutes. Additionally, both medications have side effects. Terbutaline is associated with maternal tachycardia, hyperglycemia, hypokalemia, pulmonary edema, cardiac arrhythmias, hypertension and myocardial ischemia, and NTGL is associated with maternal nausea, vomiting, headache, and hypotension. For both medications the side effects are self- limiting but depending on the patient's co-morbidities one drug may be beneficial for that individual patient. To date no study has compared the efficacy of intravenous terbutaline versus intravenous NTGL in women presenting for ECV. The purpose of this study is to determine if the success rate of ECV can be improved with the use of IV NTGL.

Interventions

DRUGIntravenous Terbutaline

0.25 mL of Intravenous Terbutaline. This will be followed 3 minutes later by an injection of 0.25 mL IV of normal saline.

DRUGIntravenous Nitroglycerine

The dose of IV nitroglycerine will be 100 micrograms three minutes before beginning the procedure, and because of it's short half-life (approximately 3 minutes) will be followed by a second dose 3 minutes later just after the start of the procedure for a total of 200 micrograms.

Sponsors

Yaakov Beilin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Female * Between 18-35 years of age * 37 weeks gestation * Breech presentation

Exclusion criteria

* Patients with ruptured membranes * Multiple gestation * Maternal age (age \> 35) * With known medical comorbidities (including hypertension (HTN), arrhythmias, endocrinologic diseases such as diabetes and thyroid disease, scoliosis, asthma) * Allergies to nitroglycerine or terbutaline * Prior abdominal or uterine surgery

Design outcomes

Primary

MeasureTime frameDescription
Successful Version of the Fetus Into the Vertex Positionaverage of 1 hourNumber of participants that had successful version of the fetus into the vertex position.

Secondary

MeasureTime frameDescription
Hypotensionaverage of 1 hourNumber of participants with hypotension
Need for Cesarean Deliveryaverage of 1 hourNumber of participants that needed a cesarean delivery
Tachycardiaaverage of 1 hourNumber of participants that had tachycardia

Countries

United States

Participant flow

Recruitment details

6 Participants were enrolled from 06/12/2014 to 05/12/2015.

Participants by arm

ArmCount
Intravenous Terbutaline
0.25 mL of Intravenous Terbutaline Intravenous Terbutaline: 0.25 mL of Intravenous Terbutaline. This will be followed 3 minutes later by an injection of 0.25 mL IV of normal saline.
3
Intravenous Nitroglycerine
IV nitroglycerine 100 micrograms three minutes before beginning the procedure, then followed by a second dose 3 minutes later just after the start of the procedure for a total of 200 micrograms. Intravenous Nitroglycerine: The dose of IV nitroglycerine will be 100 micrograms three minutes before beginning the procedure, and because of it's short half-life (approximately 3 minutes) will be followed by a second dose 3 minutes later just after the start of the procedure for a total of 200 micrograms.
2
Total5

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject01

Baseline characteristics

CharacteristicIntravenous TerbutalineIntravenous NitroglycerineTotal
Age, Continuous32 years
STANDARD_DEVIATION 1
36 years
STANDARD_DEVIATION 2
34 years
STANDARD_DEVIATION 3
Sex: Female, Male
Female
3 Participants2 Participants5 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 30 / 2
other
Total, other adverse events
0 / 30 / 2
serious
Total, serious adverse events
0 / 30 / 2

Outcome results

Primary

Successful Version of the Fetus Into the Vertex Position

Number of participants that had successful version of the fetus into the vertex position.

Time frame: average of 1 hour

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intravenous TerbutalineSuccessful Version of the Fetus Into the Vertex Position3 Participants
Intravenous NitroglycerineSuccessful Version of the Fetus Into the Vertex Position0 Participants
Secondary

Hypotension

Number of participants with hypotension

Time frame: average of 1 hour

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intravenous TerbutalineHypotension2 Participants
Intravenous NitroglycerineHypotension1 Participants
Secondary

Need for Cesarean Delivery

Number of participants that needed a cesarean delivery

Time frame: average of 1 hour

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intravenous TerbutalineNeed for Cesarean Delivery0 Participants
Intravenous NitroglycerineNeed for Cesarean Delivery0 Participants
Secondary

Tachycardia

Number of participants that had tachycardia

Time frame: average of 1 hour

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intravenous TerbutalineTachycardia2 Participants
Intravenous NitroglycerineTachycardia0 Participants

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