CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 132 enrolled
Drug / intervention
IV Acetaminophen +1 moredrug
Likely dose
IV Acetaminophen 1000mgfrom 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/NCT02046382
NCT02046382Phase 4Completed
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Randomized Control Trial of IV Acetaminophen for Post Cesarean Delivery Pain Relief

TriHealth Inc.·interventional·Posted Jan 27, 2014·Updated Aug 16, 2018

In Brief

A Phase 4 clinical trial evaluating IV Acetaminophen and Placebo for Cesarean Section and Pain, Postoperative. Completed, enrolled 132 participants across 1 site.

Detailed Summary

This study is being done to evaluate the scheduled use of intravenous (IV) acetaminophen among cesarean section patients. The study hopes to find out if patients who receive scheduled IV acetaminophen for 48 hours following delivery have lower self-reported pain scores and use less narcotic pain medication than patients who do not receive IV acetaminophen.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCesarean Section, Pain, Postoperative
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJan 27, 2014
Enrollment StartJan 1, 2014
Primary CompletionDec 1, 2016
Study CompletionMay 1, 2017
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 12.4 years ago

Interventions

IV Acetaminophendrug

1000mg dose of IV acetaminophen in 100mL solution every 8 hours for 48 hours. The first dose will be administered intraoperatively following delivery of the baby. A total of 6 doses will be given.

Placebodrug

100 mL of Normal Saline every 8 hours for 48 hours. The first does will be administered intraoperatively following delivery of the baby. A total of 6 doses will be given.