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COMPLETED
NCT05761574
PHASE3

A Study of an Acetaminophen/Naproxen Sodium Fixed Combination, Acetaminophen and Naproxen Sodium in Postoperative Dental Pain

Sponsor: Johnson & Johnson Consumer Inc. (J&JCI)

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate how well a fixed combination of acetaminophen/naproxen sodium relieves postoperative dental pain compared with acetaminophen, naproxen sodium and placebo.

Official title: A Full-Factorial, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Single-Dose Efficacy and Safety Study of an Acetaminophen/Naproxen Sodium Fixed Combination, Acetaminophen, and Naproxen Sodium in Postoperative Dental Pain

Key Details

Gender

All

Age Range

16 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

447

Start Date

2023-05-22

Completion Date

2024-05-30

Last Updated

2026-11-03

Healthy Volunteers

No

Conditions

Interventions

DRUG

Acetaminophen/Naproxen Sodium Fixed Combination

Fixed combination of Acetaminophen/Naproxen Sodium will be administered orally.

DRUG

Naproxen Sodium

Naproxen Sodium will be administered orally.

DRUG

Acetaminophen

Acetaminophen will be administered orally.

DRUG

Placebo

Placebo will be administered orally.

Locations (1)

JBR Clinical Research LLC

Salt Lake City, Utah, United States