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The Effects of Increased IV Hydration on Nulliparous Women Undergoing an Induction of Labor

NCT02989571 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2023-01-20

No results posted yet for this study

Summary

The objective of this study is to compare the effects of intravenous fluid rate on the course of labor in nulliparous patients who are undergoing labor induction and have an unfavorable cervix. The primary hypothesis is that an increased rate of intravenous fluids will shorten the length of labor in patients undergoing induction with an unfavorable cervix.

Conditions

  • Labor; Forced or Induced, Affecting Fetus or Newborn

Interventions

DRUG

Intravenous normal saline administered at 250ml/hr

Intravenous normal saline administered at 250ml/hr

DRUG

Intravenous normal saline administered at 125ml/hr

Intravenous normal saline administered at 125ml/hr

Sponsors & Collaborators

  • MemorialCare Health System

    lead OTHER

Principal Investigators

  • Vineet Shrivastava, MD · Magella Medical Group

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02989571 on ClinicalTrials.gov