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An Open-Label Study Of Celecoxib In Patients With Posttraumatic Pain

2014-08-27 03:19:23 | BioPortfolio

Summary

To investigate efficacy, safety and tolerability of Celecoxib in patients with posttraumatic pain for the duration of 8 days.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Pain

Intervention

Celecoxib

Location

Pfizer Investigational Site
Funabashi
Chiba
Japan

Status

Completed

Source

Pfizer

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:19:23-0400

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