Labor Clinical Trial
— SOFTOfficial title:
Study of Obstetric Foley Therapy (SOFT Trial)
Verified date | May 2017 |
Source | Loyola University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this study is to compare two clinically-relevant bladder drainage techniques. This is a randomized controlled trial with a single primary outcome of time to delivery. The results will inform clinical decisions about method of catheterization during labor.
Status | Completed |
Enrollment | 139 |
Est. completion date | December 2009 |
Est. primary completion date | December 2009 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Women who present to either Loyola University Medical Center or Loyola at Gottlieb Hospital in active labor or for induction of labor with a singleton pregnancy and who are anticipated to undergo vaginal delivery during the current admission Exclusion Criteria: - Women who are undergoing a scheduled cesarean delivery - Women with a contraindication to either of the 2 study interventions - Multi-fetal gestations - Current or planned tocolysis - Women who are on magnesium prophylaxis |
Country | Name | City | State |
---|---|---|---|
United States | Loyola University Health System | Maywood | Illinois |
Lead Sponsor | Collaborator |
---|---|
Loyola University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to Delivery (by Any Route) | Time to delivery defined as IV placement to delivery of infant. | 1 day | |
Secondary | Difference in Cost Between the Two Interventions | Cost of the intermittent vs. foley catheterization procedures was measured and reported in mean dollars. | End of study. |
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