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NCT03822052 · ClinicalTrials.gov registry record · NA
The Use of D5LR Versus LR for Induction of Labor and Time to Delivery in Multiparous and Primiparous Patient's With Favorable and Unfavorable Bishop's Scores
A NA study, sponsored by Ascension Health.
- Completed
- Registry status
- NA
- Development phase
- 39
- Enrollment target
NCT03822052 is a NA study that has completed, run by Ascension Health. The registered enrollment target is 39 participants.
The verdict
NCT03822052, a NA study, has completed, sponsored by Ascension Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 39 participants
- Enrollment target
Study Summary
Currently, the optimum IV fluid for induction of labor is unknown. The goal of this study is to determine the optimum fluid for induction of labor, D5LR versus LR. The investigators hypothesize that patients assigned to the D5LR group will have a shorter induction of labor when compared to patient's in the LR group.
Interventions
- OTHER Lactated ringers
- OTHER 5% dextrose lactated ringers
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 39 participants |
| Start Date | 2019-03-15 |
| Est. Completion | 2019-12-19 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03822052
The ClinicalTrials.gov registry entry for NCT03822052 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 39 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ascension Health, which has 10 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Lactated ringers is the first listed.
NCT03822052 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03822052 about?
NCT03822052 is a clinical study titled "The Use of D5LR Versus LR for Induction of Labor and Time to Delivery in Multiparous and Primiparous Patient's With Favorable and Unfavorable Bishop's Scores". Currently, the optimum IV fluid for induction of labor is unknown. The goal of this study is to determine the optimum fluid for induction of labor, D5LR versus LR. The investigators hypothesize that patients assigned to the D5LR group will have a shorter induction of labor when compared to patient's...
What is the current status of trial NCT03822052?
This trial is currently completed. It is a NA study. The enrollment target is 39 participants. The study started on 2019-03-15. Estimated completion is 2019-12-19.
What interventions are being tested in trial NCT03822052?
The interventions under investigation include: Lactated ringers (OTHER), 5% dextrose lactated ringers (OTHER).
Who is sponsoring clinical trial NCT03822052?
This trial is sponsored by Ascension Health, which has 10 total clinical trials registered on ClinicalTrials.gov.
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