NCT00426985

Brief Summary

The purpose of this study is to evaluate the effect of a ketoprofen topical patch on the pain associated with tendonitis or bursitis of the shoulder, elbow or knee

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
381

participants targeted

Target at P50-P75 for phase_3

Timeline
Completed

Started Feb 2007

Shorter than P25 for phase_3

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 24, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 26, 2007

Completed
12 days until next milestone

Study Start

First participant enrolled

February 7, 2007

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 10, 2008

Completed
Last Updated

May 5, 2026

Status Verified

August 1, 2008

Enrollment Period

1.1 years

First QC Date

January 24, 2007

Last Update Submit

April 30, 2026

Conditions

TendonitisBursitis

Keywords

TendonitisBursitisPainShoulder PainElbow PainKnee PainTendon InjuryMuscle, Bone and Cartilage Disorders

Outcome Measures

Primary Outcomes (1)

  • Average pain intensity during daily activities

Secondary Outcomes (1)

  • Average pain intensity while at rest; use of prn rescue medication; patient's and physician's global assessments of study medication, MPI, Sleep

Study Arms (2)

Ketoprofene

EXPERIMENTAL
Drug: Ketoprofen Topical Patch 20%

Placebo

PLACEBO COMPARATOR
Other: Placebo

Interventions

Ketoprofen Topical Patch 20%DRUG
Ketoprofene
PlaceboOTHER
Placebo

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Males or females 18 years of age or older
  • Diagnosis of tendonitis or bursitis of the shoulder, elbow or knee
  • Meet pain entry criteria
  • Willing to discontinue use of any pain medication not provided by study

You may not qualify if:

  • Have tendonitis or bursitis secondary to a systemic inflammatory disease, calcification or requiring surgery
  • Have received corticosteroids in the 30 days preceding screening
  • Have a history or physical examination finding that is incompatible with safe participation in the study
  • Have a history or physical examination finding that is incompatible with study product use
  • Are taking medications or other substances contraindicated due to the nature of the study medication or the potential for drug interactions.
  • Are taking medications that may significantly affect renal function

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

PPD

Austin, Texas, United States

Location

MeSH Terms

Conditions

TendinopathyBursitisPainShoulder PainTendon InjuriesCartilage Diseases

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesWounds and InjuriesJoint DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsArthralgiaConnective Tissue DiseasesSkin and Connective Tissue Diseases

Study Officials

  • PPD

    PPD Development, LP

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 24, 2007

First Posted

January 26, 2007

Study Start

February 7, 2007

Primary Completion

March 10, 2008

Study Completion

March 10, 2008

Last Updated

May 5, 2026

Record last verified: 2008-08

Locations

US(1)