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NCT02487303 · ClinicalTrials.gov registry record · NA
Intravenous Versus Oral Acetaminophen for Postoperative Pain Control After Cesarean Delivery
A NA study, sponsored by Medical University of South Carolina.
- Completed
- Registry status
- NA
- Development phase
- 148
- Enrollment target
NCT02487303 is a NA study that has completed, run by Medical University of South Carolina. The registered enrollment target is 148 participants.
The verdict
NCT02487303, a NA study, has completed, sponsored by Medical University of South Carolina.
- COMPLETED
- Registry status
- NA
- Development phase
- 148 participants
- Enrollment target
Study Summary
This study will compare IV (intravenous) versus oral (PO) acetaminophen for postoperative pain after scheduled, elective Cesarean delivery. All patients will receive a standardized spinal anesthetic for operative anesthesia and will be randomized into one of three groups: (group 1) 1 gram IV acetaminophen every 8 hours for three doses, (group 2) 1 gram oral acetaminophen every 8 hours for three doses, or (group 3) no acetaminophen. This will be a randomized, open label study.
Interventions
- DRUG Acetaminophen Intravenous
- DRUG Acetaminophen Oral
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 148 participants |
| Start Date | 2015-03-17 |
| Est. Completion | 2017-07-27 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02487303
The ClinicalTrials.gov registry entry for NCT02487303 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 148 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical University of South Carolina, which has 755 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Acetaminophen Intravenous is the first listed.
NCT02487303 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02487303 about?
NCT02487303 is a clinical study titled "Intravenous Versus Oral Acetaminophen for Postoperative Pain Control After Cesarean Delivery". This study will compare IV (intravenous) versus oral (PO) acetaminophen for postoperative pain after scheduled, elective Cesarean delivery. All patients will receive a standardized spinal anesthetic for operative anesthesia and will be randomized into one of three groups: (group 1) 1 gram IV acetami...
What is the current status of trial NCT02487303?
This trial is currently completed. It is a NA study. The enrollment target is 148 participants. The study started on 2015-03-17. Estimated completion is 2017-07-27.
What interventions are being tested in trial NCT02487303?
The interventions under investigation include: Acetaminophen Intravenous (DRUG), Acetaminophen Oral (DRUG).
Who is sponsoring clinical trial NCT02487303?
This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.
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