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NCT02837952 · ClinicalTrials.gov registry record · Phase 3

A Study of Ibuprofen (IBU) 250mg/APAP 500mg In The Treatment Of Post-Surgical Dental Pain

A Phase 3 study of Pain, sponsored by Pfizer.

Completed
Registry status
Phase 3
Development phase
123
Enrollment target
1
Study location

NCT02837952 is a Phase 3 study of Pain that has completed, run by Pfizer. The registered enrollment target is 123 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (60% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02837952, a Phase 3 study of Pain, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
123 participants
Enrollment target
1
Study location

Study Summary

This study is being conducted to determine the overall analgesic efficacy and safety of a fixed-dose ibuprofen 250 mg / acetaminophen 500 mg formulation compared to placebo in subjects who are experiencing post operative pain following surgical extraction of 3 or more third molar teeth. A review of any reported adverse events will also be completed.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG FDC IBU/APAP 250 mg/500 mg

Study Locations (1)

Utah

  • Pharmaceutical Research Associates, Inc. - Salt Lake City

Trial Details

FieldValue
Enrollment Target 123 participants
Start Date 2016-08-31
Est. Completion 2017-02-01
Phase Phase 3

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT02837952

The ClinicalTrials.gov registry entry for NCT02837952 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 123 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (60% lower). The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02837952 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.

Frequently Asked Questions

What is clinical trial NCT02837952 about?

NCT02837952 is a clinical study titled "A Study of Ibuprofen (IBU) 250mg/APAP 500mg In The Treatment Of Post-Surgical Dental Pain". This study is being conducted to determine the overall analgesic efficacy and safety of a fixed-dose ibuprofen 250 mg / acetaminophen 500 mg formulation compared to placebo in subjects who are experiencing post operative pain following surgical extraction of 3 or more third molar teeth. A review of ...

What is the current status of trial NCT02837952?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 123 participants. The study started on 2016-08-31. Estimated completion is 2017-02-01.

What conditions does trial NCT02837952 study?

This clinical trial studies the following conditions: Pain.

What interventions are being tested in trial NCT02837952?

The interventions under investigation include: Placebo (DRUG), FDC IBU/APAP 250 mg/500 mg (DRUG).

Who is sponsoring clinical trial NCT02837952?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02837952 being conducted?

This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.