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Ambulation for Obesity
N/A
Waitlist Available
Led By Ann Dude
Research Sponsored by University of Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Subjects capable of giving consent Singleton pregnancy Nulliparous (defined as no previous pregnancy beyond 20 weeks 0 days) Gestational age greater than or equal to 37 weeks BMI > = 35 at time of delivery admission Adult companion available Anticipated vaginal delivery
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 4 days postpartum
Awards & highlights
Study Summary
This trial is testing if walking with an epidural in place during labor decreases the rate of cesarean delivery in obese patients.
Eligible Conditions
- Prolonged Labor
- Obesity
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from labor onset to time of delivery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from labor onset to time of delivery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Cesarean Delivery Rate
Secondary outcome measures
First Stage Duration
Labor Duration
Perceived Labor Control
+1 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: AmbulationExperimental Treatment1 Intervention
Participants in this arm will be encouraged to ambulate with epidural in place.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ambulation
2016
N/A
~180
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Who is running the clinical trial?
University of ChicagoLead Sponsor
1,004 Previous Clinical Trials
819,763 Total Patients Enrolled
14 Trials studying Obesity
1,972 Patients Enrolled for Obesity
Ann DudePrincipal InvestigatorFaculty
Maritza GonzalezPrincipal InvestigatorFaculty
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