Diclofenac Patch for the Treatment of Acute Pain Due to Mild to Moderate Wrist Sprain, Strain or Contusion (WIND)
Primary Purpose
Acute Pain
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Diclofenac Sodium Patch
Matching Placebo Patch
Sponsored by
About this trial
This is an interventional treatment trial for Acute Pain focused on measuring wrist, sprain, strain, contusion, diclofenac, patch, acute pain, acute pain due to mild to moderate wrist sprain, strain or contusion
Eligibility Criteria
Inclusion Criteria:
- Male and female subjects 17 - 75 years of age
- Sustained recent, painful unilateral mild to moderate wrist sprain, strain or contusion
- Meet baseline pain criterion
Exclusion Criteria:
- Open wound or infection at the site of injury
- Severe wrist injury or wrist fracture
- Presence or history of hand, wrist or forearm nerve impingement or palsies
- Use of NSAIDs or opioids within 12 - 24 hours of wrist injury
- Presence or history of peptic ulcers or GI bleeding
- History of intolerance to NSAIDs, acetaminophen, adhesives
- Positive pregnancy test
- Positive drug screen
Sites / Locations
- PPD
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Diclofenac Sodium Patch
Placebo Patch
Arm Description
Outcomes
Primary Outcome Measures
Change in average pain during daily activity
Secondary Outcome Measures
Change in average pain during daily activity
Full Information
NCT ID
NCT00869063
First Posted
March 24, 2009
Last Updated
January 26, 2010
Sponsor
Cerimon Pharmaceuticals
Collaborators
PPD
1. Study Identification
Unique Protocol Identification Number
NCT00869063
Brief Title
Diclofenac Patch for the Treatment of Acute Pain Due to Mild to Moderate Wrist Sprain, Strain or Contusion
Acronym
WIND
Official Title
A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of a Diclofenac Sodium Patch for the Topical Treatment of Acute Pain Due to Mild to Moderate Wrist Sprain, Strain or Contusion
Study Type
Interventional
2. Study Status
Record Verification Date
January 2010
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
September 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Cerimon Pharmaceuticals
Collaborators
PPD
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the study is to assess the effectiveness of once daily application of a diclofenac sodium topical patch in reducing acute pain due to mild to moderate wrist sprain, strain or contusion when applied to the painful area.
Detailed Description
This randomized, double-blind, placebo-controlled, parallel group study will be conducted in patients with a mild to moderate wrist sprain, strain or contusion.
Eligible patients will be randomized (in a 1:1 ratio) to receive double-blind treatment to either the diclofenac topical patch or a matching placebo patch to be applied once daily for 7 days. Patients will return to the clinic for assessments on Day 3 and Day 7; a follow-up assessment will be conducted on Day 14. Patients will complete an electronic diary in which assessments including pain intensity, pain relief and functional disability will be recorded twice daily. Ratings of the quality of sleep will also be recorded in the diary each morning, and the use of study treatment and rescue medication will be recorded in the diary each day.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Pain
Keywords
wrist, sprain, strain, contusion, diclofenac, patch, acute pain, acute pain due to mild to moderate wrist sprain, strain or contusion
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
214 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Diclofenac Sodium Patch
Arm Type
Experimental
Arm Title
Placebo Patch
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Diclofenac Sodium Patch
Intervention Description
Topical 1% diclofenac sodium patch, applied once daily for 7 days
Intervention Type
Drug
Intervention Name(s)
Matching Placebo Patch
Intervention Description
Matching placebo patch, containing identical constituents to the active drug arm except for diclofenac sodium; applied once daily for 7 days
Primary Outcome Measure Information:
Title
Change in average pain during daily activity
Time Frame
Day 3
Secondary Outcome Measure Information:
Title
Change in average pain during daily activity
Time Frame
Day 7
10. Eligibility
Sex
All
Minimum Age & Unit of Time
17 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male and female subjects 17 - 75 years of age
Sustained recent, painful unilateral mild to moderate wrist sprain, strain or contusion
Meet baseline pain criterion
Exclusion Criteria:
Open wound or infection at the site of injury
Severe wrist injury or wrist fracture
Presence or history of hand, wrist or forearm nerve impingement or palsies
Use of NSAIDs or opioids within 12 - 24 hours of wrist injury
Presence or history of peptic ulcers or GI bleeding
History of intolerance to NSAIDs, acetaminophen, adhesives
Positive pregnancy test
Positive drug screen
Facility Information:
Facility Name
PPD
City
Austin
State/Province
Texas
ZIP/Postal Code
78704
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Diclofenac Patch for the Treatment of Acute Pain Due to Mild to Moderate Wrist Sprain, Strain or Contusion
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