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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: Completed Early Phase 1 study of Labor; Forced or Induced, Affecting Fetus or Newborn, sponsored by MemorialCare Health System.
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, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (240% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Measured via chart review
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 180 participants |
| Start Date | 2016-03 |
| Est. Completion | 2020-12 |
| Phase | Early Phase 1 |
What the finished NCT02989571 record still lists
NCT02989571 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (240% higher).
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 a single indexed study location in 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.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02989571's enrollment target sits among peer trials
180 75th of 2000 higher than 1,925 of 2,000 other Early Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Early Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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