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NCT02989571 · ClinicalTrials.gov registry record · Early Phase 1

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

A Early Phase 1 study of Labor; Forced or Induced, Affecting Fetus or Newborn, sponsored by MemorialCare Health System.

Completed
Registry status
Early Phase 1
Development phase
180
Enrollment target
1
Study location

NCT02989571 is a Early Phase 1 study of Labor; Forced or Induced, Affecting Fetus or Newborn that has completed, run by MemorialCare Health System. The registered enrollment target is 180 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT02989571, a Early Phase 1 study of Labor; Forced or Induced, Affecting Fetus or Newborn, has completed, sponsored by MemorialCare Health System.

COMPLETED
Registry status
Early Phase 1
Development phase
180 participants
Enrollment target
1
Study location

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.

Interventions

  • DRUG Intravenous normal saline administered at 250ml/hr
  • DRUG Intravenous normal saline administered at 125ml/hr

Study Locations (1)

California

  • Long Beach Memorial Medical Center - Long Beach

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2016-03
Est. Completion 2020-12
Phase Early Phase 1

Sponsor

MemorialCare Health System

21 total trials

What the Registry Record Tells You About NCT02989571

The ClinicalTrials.gov registry entry for NCT02989571 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MemorialCare Health System, which has 21 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Labor; Forced or Induced, Affecting Fetus or Newborn appearing as the primary indexed condition, and to 2 interventions - of which Intravenous normal saline administered at 250ml/hr is the first listed.

NCT02989571 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT02989571 about?

NCT02989571 is a clinical study titled "The Effects of Increased IV Hydration on Nulliparous Women Undergoing an Induction of Labor". 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...

What is the current status of trial NCT02989571?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 180 participants. The study started on 2016-03. Estimated completion is 2020-12.

What conditions does trial NCT02989571 study?

This clinical trial studies the following conditions: Labor; Forced or Induced, Affecting Fetus or Newborn.

What interventions are being tested in trial NCT02989571?

The interventions under investigation include: Intravenous normal saline administered at 250ml/hr (DRUG), Intravenous normal saline administered at 125ml/hr (DRUG).

Who is sponsoring clinical trial NCT02989571?

This trial is sponsored by MemorialCare Health System, which has 21 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02989571 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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