At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 183 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.
Intravenous Acetaminophen Versus Saline in Postoperative Analgesia After Laparoscopic Hysterectomy: A Randomized, Double Blind, Placebo Controlled Trial
In Brief
A Phase 4 clinical trial evaluating IV acetaminophen and placebo for Pain. Completed, enrolled 183 participants across 1 site.
Detailed Summary
The objective of this study is to quantify the change in post-operative pain scores and narcotic requirements in women receiving pre and post-operative IV acetaminophen compared to placebo in women undergoing laparoscopic hysterectomy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain
CountriesUnited States
Collaborators--
Timeline
Phase 4CompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartFeb 2015
First PostedMar 2015
Primary CompletionSep 2016
TodayJul 2026
First PostedMar 27, 2015
Enrollment StartFeb 1, 2015
Primary CompletionSep 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 11.3 years ago
Interventions
IV acetaminophendrug
The patients in the treatment arm will receive 1000mg of IV acetaminophen.
placebodrug
The patients in the placebo arm will receive normal saline.