CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 148 enrolled
Drug / intervention
Acetaminophen Intravenous +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02487303
NCT02487303N/ACompleted
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Intravenous Versus Oral Acetaminophen for Postoperative Pain Control After Cesarean Delivery

Medical University of South Carolina·interventional·Posted Jul 1, 2015·Updated Dec 5, 2018

In Brief

A clinical study evaluating Acetaminophen Intravenous and Acetaminophen Oral for Pain, Postoperative. Completed, enrolled 148 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain, Postoperative
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJul 1, 2015
Enrollment StartMar 17, 2015
Primary CompletionJul 27, 2017
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 11.0 years ago

Interventions

Acetaminophen Intravenousdrug

IV 1 gram f3 doses over 24 hours

Acetaminophen Oraldrug

Oral 1 gram 3 doses over 24 hours