Intravenous (IV) Nitroglycerin for Versions in Nulliparous Women (INVERT (01))
Primary Purpose
Breech Presentation, Complication of Pregnancy
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
IV Nitroglycerin
Normal saline
Sponsored by
About this trial
This is an interventional treatment trial for Breech Presentation
Eligibility Criteria
Inclusion Criteria:
- any non-cephalic presentation
- singleton pregnancy
- >/= 37 weeks gestational age
- normal amniotic fluid volume
- reassuring fetal heart rate
Exclusion Criteria:
- labor
- ruptured membranes
- history of third trimester bleeding
- any pre-existing uterine scar
- pregnancy induced hypertension and gestational diabetes
- oligohydramnios and polyhydramnios
- intrauterine growth restriction or macrosomia
- hypotension or any serious medical illness
- inability to comprehend the consent form
Sites / Locations
- Foothills Medical Centre
- Peter Lougheed Centre
- Rockyview Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
1
2
Arm Description
Treatment solution consisted of 100 micrograms/mL of nitroglycerin. After an initial 1ml dose, further doses could be given in 1-3mL increments until uterine relaxation was achieved, or up to a recommended maximum of 10mL
Placebo solution was saline. After an initial 1ml dose, further doses could be given in 1-3mL increments until uterine relaxation was achieved, or up to a recommended maximum of 10mL
Outcomes
Primary Outcome Measures
Success of ECV (ie fetus turned from Breech to cephalic) at the end of ECV procedure
Secondary Outcome Measures
Success of ECV (ie fetus in cephalic presentation) at time of delivery
Mode of delivery
Maternal side effects and adverse events
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00896311
Brief Title
Intravenous (IV) Nitroglycerin for Versions in Nulliparous Women
Acronym
INVERT (01)
Official Title
INVERT: IV Nitroglycerin for Versions Trial - a Randomized Placebo-controlled Trial in Nulliparous Women
Study Type
Interventional
2. Study Status
Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
March 2003 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
February 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of Calgary
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Breech presentations (where a baby presents with feet or bottom down) have an increased risk of perinatal and neonatal complications, and are usually delivered by cesarean section. As an alternative, so that the baby can be delivered vaginally, an attempt can be made to turn the baby so that it is head down: this manoeuvre is called an external cephalic version (ECV).
Drugs that relax the uterus (tocolytic agents) are sometimes used to help improve ECV success rates. Nitroglycerin is a tocolytic agent, but intravenous nitroglycerin has not been tested as an agent to help ECV. There is some suggestion that nitroglycerin may be more helpful in women who have not previously been pregnant (nulliparous women) than in women who have been pregnant more than once (multiparous women), and so we have planned two trials.
This study is designed to answer the following questions for nulliparous women:
Will administration of IV nitroglycerin for uterine relaxation improve ECV success rates? Will an increase in ECV success result in a decreased cesarean section rate?
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breech Presentation, Complication of Pregnancy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
82 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Treatment solution consisted of 100 micrograms/mL of nitroglycerin. After an initial 1ml dose, further doses could be given in 1-3mL increments until uterine relaxation was achieved, or up to a recommended maximum of 10mL
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo solution was saline. After an initial 1ml dose, further doses could be given in 1-3mL increments until uterine relaxation was achieved, or up to a recommended maximum of 10mL
Intervention Type
Drug
Intervention Name(s)
IV Nitroglycerin
Intervention Description
IV injection, initial dose of 1ml, with further doses of 1-3mL, up to a recommended maximum of 10mL
Intervention Type
Drug
Intervention Name(s)
Normal saline
Intervention Description
IV injection, initial dose of 1ml, with further doses of 1-3mL, up to a recommended maximum of 10mL
Primary Outcome Measure Information:
Title
Success of ECV (ie fetus turned from Breech to cephalic) at the end of ECV procedure
Time Frame
Recorded at finish of ECV attempt
Secondary Outcome Measure Information:
Title
Success of ECV (ie fetus in cephalic presentation) at time of delivery
Time Frame
Recorded at time of birth
Title
Mode of delivery
Time Frame
Recorded at time of birth
Title
Maternal side effects and adverse events
Time Frame
Recorded until date of birth (up to 3 weeks following ECV)
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
any non-cephalic presentation
singleton pregnancy
>/= 37 weeks gestational age
normal amniotic fluid volume
reassuring fetal heart rate
Exclusion Criteria:
labor
ruptured membranes
history of third trimester bleeding
any pre-existing uterine scar
pregnancy induced hypertension and gestational diabetes
oligohydramnios and polyhydramnios
intrauterine growth restriction or macrosomia
hypotension or any serious medical illness
inability to comprehend the consent form
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruce B Allan, MD PhD
Organizational Affiliation
Calgary Health Region
Official's Role
Principal Investigator
Facility Information:
Facility Name
Foothills Medical Centre
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 4J8
Country
Canada
Facility Name
Peter Lougheed Centre
City
Calgary
State/Province
Alberta
Country
Canada
Facility Name
Rockyview Hospital
City
Calgary
State/Province
Alberta
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
19701035
Citation
Hilton J, Allan B, Swaby C, Wah R, Jarrell J, Wood S, Ross S, Tran Q. Intravenous nitroglycerin for external cephalic version: a randomized controlled trial. Obstet Gynecol. 2009 Sep;114(3):560-567. doi: 10.1097/AOG.0b013e3181b05a19. Erratum In: Obstet Gynecol. 2009 Nov;114(5):1148. Wah, Raouf [corrected to Wahba, Raouf].
Results Reference
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Intravenous (IV) Nitroglycerin for Versions in Nulliparous Women
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