Trials / Terminated
TerminatedNCT00259519
Safety and Efficacy Study of Intentional Delivery in Women With Preterm and Prelabour Rupture of the Membranes
Effects of Intentional Delivery After Preterm and Prelabor Rupture of Membranes Between 32 and 35 Weeks of Gestation: A Multicentre Randomized and Controlled Trial
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 152 (actual)
- Sponsor
- University of Alberta · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Two-year multicentre randomized controlled parallel trial to compare intentional delivery and conservative management in pregnant women with preterm and prelabour rupture of membranes between 32 and 35 weeks. The purpose of this study is to determine whether intentional delivery of women with PPROM between 32 and 35 week's gestation can decrease the overall neonatal morbidity associated with PPROM-related complications without increasing the morbidity associated with a shortened pregnancy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Induction of delivery | Induction of delivery |
Timeline
- Start date
- 2006-01-01
- Primary completion
- 2010-03-01
- Completion
- 2020-03-01
- First posted
- 2005-11-29
- Last updated
- 2020-03-25
Locations
11 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT00259519. Inclusion in this directory is not an endorsement.