Clinical trial
Safety and Efficacy Study of Intentional Delivery in Women With Preterm and…
NCT00259519 · University of Alberta, Other · Terminated
Key facts
| NCT number | NCT00259519 |
|---|---|
| Title | Safety and Efficacy Study of Intentional Delivery in Women With Preterm and Prelabour Rupture of the Membranes |
| Official title | Effects of Intentional Delivery After Preterm and Prelabor Rupture of Membranes Between 32 and 35 Weeks of Gestation: A Multicentre Randomized and Controlled Trial |
| Lead sponsor | University of Alberta, Other |
| Collaborators | Stollery Children's Hospital Foundation |
| Status | Terminated |
| Study type | Interventional |
| Conditions | Fetal Membranes, Premature Rupture |
| Intervention type | Procedure |
| Interventions | Induction of delivery |
| Enrollment | 152 |
| Start date | Jan 1, 2006 |
| Primary completion | Mar 1, 2010 |
| Completion | Mar 1, 2020 |
| First posted | Nov 29, 2005 |
| Last update posted | Mar 25, 2020 |
| Countries | Canada |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: