Mild Preeclampsia Near Term: Deliver or Deliberate?
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|ClinicalTrials.gov Identifier: NCT00789919|
Recruitment Status : Completed
First Posted : November 13, 2008
Last Update Posted : February 10, 2017
|Condition or disease||Intervention/treatment||Phase|
|Preeclampsia||Procedure: Delivery of infant||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||185 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Mild Preeclampsia Near Term: Deliver or Deliberate?|
|Study Start Date :||March 2002|
|Actual Primary Completion Date :||July 2008|
|Actual Study Completion Date :||July 2008|
No Intervention: 1
Study participants (those diagnosed with mild preeclampsia) are admitted to hospital for standard inpatient management of their disease.
Study participants (those diagnosed with mild preeclampsia) are admitted to hospital and their infant is delivered as soon as possible after 34 weeks gestation. As there is no determined optimal time of delivery in these patients, delivery is the intervention.
Procedure: Delivery of infant
Vaginal delivery or cesarean section, whichever is indicated
- Progression to severe preeclampsia in the control group necessitating delivery of the infant. [ Time Frame: End of study ]
- Maternal morbidity [ Time Frame: End of study ]
- Fetal morbidity and mortality [ Time Frame: End of study ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00789919
|United States, Mississippi|
|Winfred L Wiser Hospital for Women and Infants|
|Jackson, Mississippi, United States, 39216|
|Principal Investigator:||Michelle Y Owens, M.D.||University of Mississippi Medical Center|