At a glance

ClinicalIndex Comparison Record

Phase 3Completed· 244 enrolled

Drug / intervention

IV Placebo +3 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/NCT00564486

NCT00564486Phase 3Completed

Compare CT.gov

Phase 3 Randomized, Double-Blind Placebo-Controlled, Multicenter, Parallel-Group, Repeated-Dose Study of the Analgesic Efficacy & Safety of IV Acetaminophen Versus Placebo for the Treatment of Postop Pain

Mallinckrodt·interventional·Posted Nov 28, 2007·Updated Oct 21, 2016

In Brief

A Phase 3 clinical trial evaluating IV Placebo and IV Acetaminophen for Pain. Completed, enrolled 244 participants across 17 sites.

Detailed Summary

This research study will look at the pain relieving ability and safety of using repeated doses of intravenous (into the vein \[IV\]) acetaminophen in the treatment of moderate postoperative pain after planned or elective abdominal laparoscopic surgery, such as a laparoscopic abdominal hysterectomy or laparoscopic cholecystectomy (removal of the gall bladder).

Study Details

Study Typeinterventional

Allocation--

Masking--

Primary Purpose--

ConditionsPain

CountriesUnited States

Collaborators--

Timeline

Phase 3CompletedFinished

20082009201020112012201320142015201620172018201920202021202220232024202520262027

Enrollment StartNov 2007

First PostedNov 2007

Primary CompletionSep 2008

TodayJul 2026

First PostedNov 28, 2007

Enrollment StartNov 1, 2007

Primary CompletionSep 1, 2008

TodayJul 2, 2026

Enrollment to primary: 10 monthsPosted 18.6 years ago

Interventions

IV Placebodrug

IV, every 6 hours for 24 hours (4 doses total)

IV Placebodrug

IV, every 4 hours for 24 hours (6 doses total)

IV Acetaminophendrug

IV, every 6 hours for 24 hours (4 doses total)

IV Acetaminophendrug

IV, every 4 hours for 24 hours (6 doses total)