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Safety and Efficacy Study of Intentional Delivery in Women With Preterm and Prelabour Rupture of the Membranes

Fetal Membranes, Premature Rupture Clinical Trial

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

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Fetal Membranes, Premature Rupture
  • Rupture
Clinical Trial Details
NCT number NCT00259519
Study type Interventional
Source University of Alberta
Contact
Status Terminated
Phase N/A
Start date January 2006
Completion date March 2020
View Details
See also
  Status Clinical Trial Phase
Terminated NCT00201656 - Removal Versus Retention of Cerclage in Preterm Premature Rupture of Membranes (PPROM) Phase 4
Completed NCT02901795 - Early Detection of Chorioamnionitis in Preterm Premature Rupture of Membranes
Not yet recruiting NCT00247104 - The Use of Cranberries in Women With Preterm Premature Rupture of Membranes N/A
Not yet recruiting NCT06262308 - Emotional Support for Women Experiencing PPROM N/A
Recruiting NCT02380560 - Myometrial Thickness as a Predictor for the Latency Interval in PPROM N/A
Completed NCT00070746 - Perinatal Infections in Pakistan N/A
Recruiting NCT02997345 - PPROM Registry (Preterm Premature Rupture of Membranes)
Terminated NCT00290199 - Foley Catheter for Labor Induction in Women With Term and Near Term Membrane Rupture N/A
Recruiting NCT02369601 - PROMComplete for Determination of Rupture of Fetal Membranes
Terminated NCT00890630 - Intracervical Catheters for Induction of Labour in Women With Prelabour Rupture of Membranes at Term Phase 2
Withdrawn NCT01063686 - The Cervical Cap in the Diagnosis of Rupture of Membranes in the Second Trimester N/A
Not yet recruiting NCT00432588 - Comparing the Effect of Vaginal Misoprostol With Dinoprostone in Term Pregnancies Phase 1/Phase 2