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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
No Placebo-Only Group

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 weeks
Treatment ~ Varies
Follow Up ~5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 5 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
rate of cesarean section
Secondary study objectives
labor
Other study objectives
Maternal complications (as diagnosed by managing clinician, (n/%) for all)
Neonatal outcomes (as diagnosed by managing clinician, (n/%) for all)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial 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
~55 spots leftby Nov 2025
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