The Canadian preterm labour nitroglycerin trial
- Conditions
- Preterm labourPregnancy and Childbirth
- Registration Number
- ISRCTN20129681
- Lead Sponsor
- Queen's University (Canada)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 600
1. Greater than or equal to 24 to less than or equal to 32 weeks gestational age based on menstrual dates or earliest ultrasound scan
2. Preterm labour:
2.1. At least four painful uterine contractions per 20 minutes
2.2. Change in the cervix (change in bishop score or bishop score greater than or equal to 6)
1. Any maternal (e.g. significant antepartum haemorrhage) or foetal (e.g. non-reassuring heart rate pattern) condition necessitating immediate delivery
2. Multiple gestations (i.e. twins, triplets etc.)
3. Premature prelabour rupture of the membranes (PPROM)
4. Intrauterine foetal demise or lethal foetal anomalies
5. Cervix dilated greater than 8 cm
6. Treatment with another agent within 24 hours
7. Previous enrolment in this trial
8. Known sensitivity to GTN
9. Failure to give consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method