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Diclofenac Patch for Treatment of Acute Pain Due to Mild to Moderate Soft Tissue Injuries (TAPED)

NCT00931866 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 407

Last updated 2010-08-16

No results posted yet for this study

Summary

The primary purpose of this study is to assess the effectiveness of once daily application of a diclofenac sodium topical patch in reducing mild to moderate soft tissue injuries when applied to the painful area.

Conditions

  • Acute Pain
  • Soft Tissue Injury

Interventions

DRUG

Diclofenac Sodium

Topical diclofenac patch applied once daily to area of pain

DRUG

Matching Placebo Patch

Matching placebo patch, containing identical constituents to the active comparator except for diclofenac sodium; applied once daily

Sponsors & Collaborators

  • PPD Development, LP

    collaborator INDUSTRY

  • Cerimon Pharmaceuticals

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2009-09-30
Completion
2009-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00931866 on ClinicalTrials.gov