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Intervention for Pregnancy
N/A
Waitlist Available
Led By Suneet P Chauhan, MD
Research Sponsored by Chauhan, Suneet P., M.D.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 years
Awards & highlights
Study Summary
The hypothesis of the present study is the hydration of nulliparous women with 250ml/hour vs. 125ml/hrs would decrease the rate of primary cesarean section.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
rate of cesarean section
Secondary outcome measures
labor
Other outcome measures
Maternal complications (as diagnosed by managing clinician, (n/%) for all)
Neonatal outcomes (as diagnosed by managing clinician, (n/%) for all)
The indication for cesarean delivery (n/%) versus The indication for operative vaginal delivery (n/%)
+5 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
IV Hydration at 250 cc hour
Group II: RoutineActive Control1 Intervention
IV Hydration at 125 cc hour
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Who is running the clinical trial?
Chauhan, Suneet P., M.D.Lead Sponsor
Suneet P Chauhan, MDPrincipal Investigator
Andrew Combs, MD PhDPrincipal InvestigatorObstetrix Medical Group
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