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NCT02267772 · ClinicalTrials.gov registry record · NA
IV Acetaminophen vs IV Morphine for Pain Control in Pregnant Women
A NA study, sponsored by The University of Texas Health Science Center, Houston.
- Terminated
- Registry status
- NA
- Development phase
- 163
- Enrollment target
NCT02267772 is a NA study that was terminated before completion, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 163 participants.
The verdict
NCT02267772, a NA study, was terminated before completion, sponsored by The University of Texas Health Science Center, Houston.
- TERMINATED
- Registry status
- NA
- Development phase
- 163 participants
- Enrollment target
Study Summary
Purpose: To determine if IV acetaminophen can 1) decrease pain in pregnancy women, 2)reduce the amount of opioid use in pregnant women who encounter pain, 3) reduce maternal and fetal adverse effects compared to opioids. Design: This is a comparative effective trial that is a randomized, controlled trial of IV acetaminophen vs. IV morphine in pregnant women. Procedures: Women meeting inclusion/exclusion criteria will be randomized to IV acetaminophen or IV morphine. The IV acetaminophen group will get up to four standard doses of IV acetaminophen during their stay at the hospital. The second group will get up to six standard doses of morphine. Subjects will complete a pain scale after medication administration and will be asked about any side effects.
Interventions
- DRUG IV Acetaminophen
- DRUG IV Morphine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 163 participants |
| Start Date | 2014-01 |
| Est. Completion | 2019-04-27 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02267772
The ClinicalTrials.gov registry entry for NCT02267772 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 163 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which IV Acetaminophen is the first listed.
NCT02267772 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02267772 about?
NCT02267772 is a clinical study titled "IV Acetaminophen vs IV Morphine for Pain Control in Pregnant Women". Purpose: To determine if IV acetaminophen can 1) decrease pain in pregnancy women, 2)reduce the amount of opioid use in pregnant women who encounter pain, 3) reduce maternal and fetal adverse effects compared to opioids. Design: This is a comparative effective trial that is a randomized, controlled...
What is the current status of trial NCT02267772?
This trial is currently terminated. It is a NA study. The enrollment target is 163 participants. The study started on 2014-01. Estimated completion is 2019-04-27.
What interventions are being tested in trial NCT02267772?
The interventions under investigation include: IV Acetaminophen (DRUG), IV Morphine (DRUG).
Who is sponsoring clinical trial NCT02267772?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
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